Canonical Allele Identifier: CA1329210885

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420555T= , CM000664.2:g.219420555T=	GRCh38
NC_000002.11:g.220285277T= , CM000664.1:g.220285277T=	GRCh37
NC_000002.10:g.219993521T=	NCBI36
NG_008043.1:g.7179T= , LRG_380:g.7179T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.270T=
ENST00000683013.1:n.184T=
ENST00000373960.4:c.796T= MANE Select	ENSP00000363071.3:p.Ser266=
ENST00000373960.3:c.796T=	ENSP00000363071.3:p.Ser266=
ENST00000477226.5:n.268T=
ENST00000492726.1:n.191T=
NM_001927.3:c.796T= , LRG_380t1:c.796T=	NP_001918.3:p.Ser266=
NM_001927.4:c.796T= MANE Select	NP_001918.3:p.Ser266=
NM_001382708.1:c.793T=	NP_001369637.1:p.Ser265=
NM_001382709.1:c.735+209T=	NP_001369638.1:n.735+209T=
NM_001382710.1:c.796T=	NP_001369639.1:p.Ser266=
NM_001382711.1:c.796T=	NP_001369640.1:p.Ser266=
NM_001382712.1:c.796T=	NP_001369641.1:p.Ser266=
NM_001382713.1:c.526T=	NP_001369642.1:p.Ser176=