Canonical Allele Identifier: CA1329211316

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421486C= , CM000664.2:g.219421486C=	GRCh38
NC_000002.11:g.220286208C= , CM000664.1:g.220286208C=	GRCh37
NC_000002.10:g.219994452C=	NCBI36
NG_008043.1:g.8110C= , LRG_380:g.8110C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.644C=
ENST00000683013.1:n.558C=
ENST00000373960.4:c.1170C= MANE Select	ENSP00000363071.3:p.Asp390=
ENST00000373960.3:c.1170C=	ENSP00000363071.3:p.Asp390=
ENST00000477226.5:n.642C=
ENST00000492726.1:n.565C=
NM_001927.3:c.1170C= , LRG_380t1:c.1170C=	NP_001918.3:p.Asp390=
NM_001927.4:c.1170C= MANE Select	NP_001918.3:p.Asp390=
NM_001382708.1:c.1167C=	NP_001369637.1:p.Asp389=
NM_001382709.1:c.738C=	NP_001369638.1:p.Asp246=
NM_001382710.1:c.1101C=	NP_001369639.1:p.Asp367=
NM_001382711.1:c.1149C=	NP_001369640.1:p.Asp383=
NM_001382712.1:c.1170C=	NP_001369641.1:p.Asp390=
NM_001382713.1:c.900C=	NP_001369642.1:p.Asp300=