Canonical Allele Identifier: CA1329211336

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421525C= , CM000664.2:g.219421525C=	GRCh38
NC_000002.11:g.220286247C= , CM000664.1:g.220286247C=	GRCh37
NC_000002.10:g.219994491C=	NCBI36
NG_008043.1:g.8149C= , LRG_380:g.8149C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.683C=
ENST00000683013.1:n.597C=
ENST00000373960.4:c.1209C= MANE Select	ENSP00000363071.3:p.Ala403=
ENST00000373960.3:c.1209C=	ENSP00000363071.3:p.Ala403=
ENST00000477226.5:n.681C=
ENST00000492726.1:n.604C=
NM_001927.3:c.1209C= , LRG_380t1:c.1209C=	NP_001918.3:p.Ala403=
NM_001927.4:c.1209C= MANE Select	NP_001918.3:p.Ala403=
NM_001382708.1:c.1206C=	NP_001369637.1:p.Ala402=
NM_001382709.1:c.777C=	NP_001369638.1:p.Ala259=
NM_001382710.1:c.1140C=	NP_001369639.1:p.Ala380=
NM_001382711.1:c.1188C=	NP_001369640.1:p.Ala396=
NM_001382712.1:c.1209C=	NP_001369641.1:p.Ala403=
NM_001382713.1:c.939C=	NP_001369642.1:p.Ala313=