Canonical Allele Identifier: CA1139837008

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158642446A= , CM000663.2:g.158642446A=	GRCh38
NC_000001.10:g.158612236A= , CM000663.1:g.158612236A=	GRCh37
NC_000001.9:g.156878860A=	NCBI36
NG_011474.1:g.49271T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.4702T= MANE Select	ENSP00000495214.1:p.Cys1568=
ENST00000368147.8:c.4702T=	ENSP00000357129.4:p.Cys1568=
ENST00000465741.1:n.87T=
ENST00000614909.4:c.4702T=	ENSP00000482595.1:p.Cys1568=
NM_003126.2:c.4702T=	NP_003117.2:p.Cys1568=
XM_011509916.1:c.4702T=	XP_011508218.1:p.Cys1568=
XM_011509917.1:c.4702T=	XP_011508219.1:p.Cys1568=
XM_011509918.1:c.4702T=	XP_011508220.1:p.Cys1568=
XM_011509919.1:c.4702T=	XP_011508221.1:p.Cys1568=
XR_921911.1:n.4815T=
XR_921912.1:n.4890T=
NM_003126.3:c.4702T=	NP_003117.2:p.Cys1568=
XM_011509916.2:c.4702T=	XP_011508218.1:p.Cys1568=
XM_011509917.3:c.4702T=	XP_011508219.1:p.Cys1568=
XM_011509918.3:c.4702T=	XP_011508220.1:p.Cys1568=
XM_011509919.3:c.4702T=	XP_011508221.1:p.Cys1568=
XR_921911.3:n.4828T=
XR_921912.2:n.4900T=
NM_003126.4:c.4702T= MANE Select	NP_003117.2:p.Cys1568=