Canonical Allele Identifier: CA1329213131

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425727C= , CM000664.2:g.219425727C=	GRCh38
NC_000002.11:g.220290449C= , CM000664.1:g.220290449C=	GRCh37
NC_000002.10:g.219998693C=	NCBI36
NG_008043.1:g.12351C= , LRG_380:g.12351C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.827C=
ENST00000683013.1:n.741C=
ENST00000373960.4:c.1353C= MANE Select	ENSP00000363071.3:p.Ile451=
ENST00000373960.3:c.1353C=	ENSP00000363071.3:p.Ile451=
ENST00000483395.1:n.208C=
NM_001927.3:c.1353C= , LRG_380t1:c.1353C=	NP_001918.3:p.Ile451=
NM_001927.4:c.1353C= MANE Select	NP_001918.3:p.Ile451=
NM_001382708.1:c.1350C=	NP_001369637.1:p.Ile450=
NM_001382709.1:c.921C=	NP_001369638.1:p.Ile307=
NM_001382710.1:c.1284C=	NP_001369639.1:p.Ile428=
NM_001382711.1:c.1332C=	NP_001369640.1:p.Ile444=
NM_001382712.1:c.1353C=	NP_001369641.1:p.Ile451=
NM_001382713.1:c.1083C=	NP_001369642.1:p.Ile361=