Canonical Allele Identifier: CA1329210882

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420552A= , CM000664.2:g.219420552A=	GRCh38
NC_000002.11:g.220285274A= , CM000664.1:g.220285274A=	GRCh37
NC_000002.10:g.219993518A=	NCBI36
NG_008043.1:g.7176A= , LRG_380:g.7176A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.267A=
ENST00000683013.1:n.181A=
ENST00000373960.4:c.793A= MANE Select	ENSP00000363071.3:p.Met265=
ENST00000373960.3:c.793A=	ENSP00000363071.3:p.Met265=
ENST00000477226.5:n.265A=
ENST00000492726.1:n.188A=
NM_001927.3:c.793A= , LRG_380t1:c.793A=	NP_001918.3:p.Met265=
NM_001927.4:c.793A= MANE Select	NP_001918.3:p.Met265=
NM_001382708.1:c.790A=	NP_001369637.1:p.Met264=
NM_001382709.1:c.735+206A=	NP_001369638.1:n.735+206A=
NM_001382710.1:c.793A=	NP_001369639.1:p.Met265=
NM_001382711.1:c.793A=	NP_001369640.1:p.Met265=
NM_001382712.1:c.793A=	NP_001369641.1:p.Met265=
NM_001382713.1:c.523A=	NP_001369642.1:p.Met175=