Canonical Allele Identifier: CA350686069

Gene: DES

Linked Data

• dbSNP Id: rs1954376103
• gnomAD v4: 2-219418887-G-A
• MyVariant Identifiers: chr2:g.220283609G>A (hg19) ; chr2:g.219418887G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219418887G>A , CM000664.2:g.219418887G>A	GRCh38
NC_000002.11:g.220283609G>A , CM000664.1:g.220283609G>A	GRCh37
NC_000002.10:g.219991853G>A	NCBI36
NG_008043.1:g.5511G>A , LRG_380:g.5511G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373960.4:c.425G>A MANE Select	ENSP00000363071.3:p.Arg142Gln
ENST00000373960.3:c.425G>A	ENSP00000363071.3:p.Arg142Gln
NM_001927.3:c.425G>A , LRG_380t1:c.425G>A	NP_001918.3:p.Arg142Gln
NM_001927.4:c.425G>A MANE Select	NP_001918.3:p.Arg142Gln
NM_001382708.1:c.425G>A	NP_001369637.1:p.Arg142Gln
NM_001382709.1:c.425G>A	NP_001369638.1:p.Arg142Gln
NM_001382710.1:c.425G>A	NP_001369639.1:p.Arg142Gln
NM_001382711.1:c.425G>A	NP_001369640.1:p.Arg142Gln
NM_001382712.1:c.425G>A	NP_001369641.1:p.Arg142Gln
NM_001382713.1:c.425G>A	NP_001369642.1:p.Arg142Gln