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a sequence change where, compared to a reference sequence, one or more nucleotides are not present (deleted).
Description
Format: “prefix”“position(s)_deleted”“del”, e.g. r.123_127del
“prefix” = reference sequence used = r. “position(s)_deleted” = position nucleotide or range of nucleotides deleted = 123_127 “del” = type of change is a deletion = del 1
Note
all variants should be described at the DNA level, descriptions at the RNA and/or protein level may be given in addition
prefix reference sequences accepted are r. (coding and non-coding RNA).
the “position(s)_deleted” should contain two different positions, e.g. 123_126 but not 123_123.
the “position(s)_deleted” should be listed from 5’ to 3’, e.g. 123_126 but not 126_123.
for all descriptions the most 3’ position possible of the reference sequence is arbitrarily assigned to have been changed (3’rule)
the 3’rule also applies for changes in single residue stretches and tandem repeats (nucleotide or amino acid)
NOTE: the exception to the 3’rule for deletions around exon/exon junctions see Deletions does not apply when describing variants based on a RNA reference sequence
1 = see Uncertain; when the postion and/or the sequence of a deletion has not been defined, a description may have a format like r.(100_150)del(15)
Examples
one nucleotide
LRG_199t1:r.10del
a deletion of the U at position r.10 in the reference sequence LRG_199t1
several nucleotides
NM_004006.2:r.6_8del
a deletion of nucleotides r.6 to r.8 in the reference sequence NM_004006.2
NOTE: it is allowed to describe the variant as r.6_8deluug
LRG_2t1:r.1034_1036del
a deletion of nucleotides r.1034 to r.1036 (“uug”) in the reference sequence LRG_2t1
NOTE: since the 3’rule has to be applied the variant, crossing the intron between nucleotides r.1035 and r.1036, is not described as r.1033_1035del (deletion “guu”)
LRG_199t1:r.(4072_5145del)
the predicted deletion of exon 30 (starting at position r.4072) to exon 36 (ending at position r.5145) of the DMD-gene; RNA has not been analysed
LRG_199t1:r.=/6_8del
a mosaic case where from position r.6 to r.8 besides the normal sequence also transcripts are found containing a deletion of this sequence
NOTE: for the predicted consequences of a variant the description is LRG_199t1:r.(=/6_8del)
Q&A
Can I use r.123del6 to describe a 6 nucleotide deletion?
No, a deletion of more than one residue should mention the first and last residue deleted, separated using the range symbol ("_", underscore), e.g. r.123_128del and not r.123del6.
Is the description of a deletion of exon 17 as r.EX17del still allowed?
A description like r.EX17del has never been allowed. Descriptions should be specific and indicate the nucleotides affected by the change.