Canonical Allele Identifier: CA1329213133

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425731A= , CM000664.2:g.219425731A=	GRCh38
NC_000002.11:g.220290453A= , CM000664.1:g.220290453A=	GRCh37
NC_000002.10:g.219998697A=	NCBI36
NG_008043.1:g.12355A= , LRG_380:g.12355A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.831A=
ENST00000683013.1:n.745A=
ENST00000373960.4:c.1357A= MANE Select	ENSP00000363071.3:p.Thr453=
ENST00000373960.3:c.1357A=	ENSP00000363071.3:p.Thr453=
ENST00000483395.1:n.212A=
NM_001927.3:c.1357A= , LRG_380t1:c.1357A=	NP_001918.3:p.Thr453=
NM_001927.4:c.1357A= MANE Select	NP_001918.3:p.Thr453=
NM_001382708.1:c.1354A=	NP_001369637.1:p.Thr452=
NM_001382709.1:c.925A=	NP_001369638.1:p.Thr309=
NM_001382710.1:c.1288A=	NP_001369639.1:p.Thr430=
NM_001382711.1:c.1336A=	NP_001369640.1:p.Thr446=
NM_001382712.1:c.1357A=	NP_001369641.1:p.Thr453=
NM_001382713.1:c.1087A=	NP_001369642.1:p.Thr363=