Canonical Allele Identifier: CA2663248302

Gene: DES

Linked Data

• dbSNP Id: rs2125166763
• gnomAD v4: 2-219419185-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219419185C>A , CM000664.2:g.219419185C>A	GRCh38
NC_000002.11:g.220283907C>A , CM000664.1:g.220283907C>A	GRCh37
NC_000002.10:g.219992151C>A	NCBI36
NG_008043.1:g.5809C>A , LRG_380:g.5809C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373960.4:c.578+145C>A MANE Select	ENSP00000363071.3:n.578+145C>A
ENST00000373960.3:c.578+145C>A	ENSP00000363071.3:n.578+145C>A
NM_001927.3:c.578+145C>A , LRG_380t1:c.578+145C>A	NP_001918.3:n.578+145C>A
NM_001927.4:c.578+145C>A MANE Select	NP_001918.3:n.578+145C>A
NM_001382708.1:c.578+145C>A	NP_001369637.1:n.578+145C>A
NM_001382709.1:c.578+145C>A	NP_001369638.1:n.578+145C>A
NM_001382710.1:c.578+145C>A	NP_001369639.1:n.578+145C>A
NM_001382711.1:c.578+145C>A	NP_001369640.1:n.578+145C>A
NM_001382712.1:c.578+145C>A	NP_001369641.1:n.578+145C>A
NM_001382713.1:c.495+228C>A	NP_001369642.1:n.495+228C>A