Canonical Allele Identifier: CA350698988

Gene: DES

Linked Data

• gnomAD v4: 2-219425961-G-T
• MyVariant Identifiers: chr2:g.220290683G>T (hg19) ; chr2:g.219425961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425961G>T , CM000664.2:g.219425961G>T	GRCh38
NC_000002.11:g.220290683G>T , CM000664.1:g.220290683G>T	GRCh37
NC_000002.10:g.219998927G>T	NCBI36
NG_008043.1:g.12585G>T , LRG_380:g.12585G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.858G>T
ENST00000683013.1:n.772G>T
ENST00000373960.4:c.1384G>T MANE Select	ENSP00000363071.3:p.Ala462Ser
ENST00000373960.3:c.1384G>T	ENSP00000363071.3:p.Ala462Ser
ENST00000483395.1:n.239G>T
NM_001927.3:c.1384G>T , LRG_380t1:c.1384G>T	NP_001918.3:p.Ala462Ser
NM_001927.4:c.1384G>T MANE Select	NP_001918.3:p.Ala462Ser
NM_001382708.1:c.1381G>T	NP_001369637.1:p.Ala461Ser
NM_001382709.1:c.952G>T	NP_001369638.1:p.Ala318Ser
NM_001382710.1:c.1315G>T	NP_001369639.1:p.Ala439Ser
NM_001382711.1:c.1363G>T	NP_001369640.1:p.Ala455Ser
NM_001382712.1:c.1371+216G>T	NP_001369641.1:n.1371+216G>T
NM_001382713.1:c.1114G>T	NP_001369642.1:p.Ala372Ser