Canonical Allele Identifier: CA1329213443

Gene: DES

Linked Data

• dbSNP Id: rs1954539460
• gnomAD v4: 2-219426427-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219426427G>A , CM000664.2:g.219426427G>A	GRCh38
NC_000002.11:g.220291149G>A , CM000664.1:g.220291149G>A	GRCh37
NC_000002.10:g.219999393G>A	NCBI36
NG_008043.1:g.13051G>A , LRG_380:g.13051G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.1324G>A
ENST00000683013.1:n.1238G>A
ENST00000373960.4:c.*437G>A MANE Select	ENSP00000363071.3:n.*437G>A
ENST00000373960.3:c.*437G>A	ENSP00000363071.3:n.*437G>A
NM_001927.3:c.*437G>A , LRG_380t1:c.*437G>A	NP_001918.3:n.*437G>A
NM_001927.4:c.*437G>A MANE Select	NP_001918.3:n.*437G>A
NM_001382708.1:c.*437G>A	NP_001369637.1:n.*437G>A
NM_001382709.1:c.*437G>A	NP_001369638.1:n.*437G>A
NM_001382710.1:c.*437G>A	NP_001369639.1:n.*437G>A
NM_001382711.1:c.*437G>A	NP_001369640.1:n.*437G>A
NM_001382712.1:c.1372-126G>A	NP_001369641.1:n.1372-126G>A
NM_001382713.1:c.*437G>A	NP_001369642.1:n.*437G>A