Canonical Allele Identifier: CA1329213120

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425708C= , CM000664.2:g.219425708C=	GRCh38
NC_000002.11:g.220290430C= , CM000664.1:g.220290430C=	GRCh37
NC_000002.10:g.219998674C=	NCBI36
NG_008043.1:g.12332C= , LRG_380:g.12332C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.808C=
ENST00000683013.1:n.722C=
ENST00000373960.4:c.1334C= MANE Select	ENSP00000363071.3:p.Thr445=
ENST00000373960.3:c.1334C=	ENSP00000363071.3:p.Thr445=
ENST00000483395.1:n.189C=
NM_001927.3:c.1334C= , LRG_380t1:c.1334C=	NP_001918.3:p.Thr445=
NM_001927.4:c.1334C= MANE Select	NP_001918.3:p.Thr445=
NM_001382708.1:c.1331C=	NP_001369637.1:p.Thr444=
NM_001382709.1:c.902C=	NP_001369638.1:p.Thr301=
NM_001382710.1:c.1265C=	NP_001369639.1:p.Thr422=
NM_001382711.1:c.1313C=	NP_001369640.1:p.Thr438=
NM_001382712.1:c.1334C=	NP_001369641.1:p.Thr445=
NM_001382713.1:c.1064C=	NP_001369642.1:p.Thr355=