Canonical Allele Identifier: CA1329213119

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425707A= , CM000664.2:g.219425707A=	GRCh38
NC_000002.11:g.220290429A= , CM000664.1:g.220290429A=	GRCh37
NC_000002.10:g.219998673A=	NCBI36
NG_008043.1:g.12331A= , LRG_380:g.12331A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.807A=
ENST00000683013.1:n.721A=
ENST00000373960.4:c.1333A= MANE Select	ENSP00000363071.3:p.Thr445=
ENST00000373960.3:c.1333A=	ENSP00000363071.3:p.Thr445=
ENST00000483395.1:n.188A=
NM_001927.3:c.1333A= , LRG_380t1:c.1333A=	NP_001918.3:p.Thr445=
NM_001927.4:c.1333A= MANE Select	NP_001918.3:p.Thr445=
NM_001382708.1:c.1330A=	NP_001369637.1:p.Thr444=
NM_001382709.1:c.901A=	NP_001369638.1:p.Thr301=
NM_001382710.1:c.1264A=	NP_001369639.1:p.Thr422=
NM_001382711.1:c.1312A=	NP_001369640.1:p.Thr438=
NM_001382712.1:c.1333A=	NP_001369641.1:p.Thr445=
NM_001382713.1:c.1063A=	NP_001369642.1:p.Thr355=