Canonical Allele Identifier: CA1201568187

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685330C= , CM000663.2:g.158685330C=	GRCh38
NC_000001.10:g.158655120C= , CM000663.1:g.158655120C=	GRCh37
NC_000001.9:g.156921744C=	NCBI36
NG_011474.1:g.6387G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.42G= MANE Select	ENSP00000495214.1:p.Gly14=
ENST00000368147.8:c.42G=	ENSP00000357129.4:p.Gly14=
ENST00000467387.1:c.42G=	ENSP00000476485.1:p.Gly14=
ENST00000614909.4:c.42G=	ENSP00000482595.1:p.Gly14=
NM_003126.2:c.42G=	NP_003117.2:p.Gly14=
XM_011509916.1:c.42G=	XP_011508218.1:p.Gly14=
XM_011509917.1:c.42G=	XP_011508219.1:p.Gly14=
XM_011509918.1:c.42G=	XP_011508220.1:p.Gly14=
XM_011509919.1:c.42G=	XP_011508221.1:p.Gly14=
XR_921911.1:n.155G=
XR_921912.1:n.160G=
NM_003126.3:c.42G=	NP_003117.2:p.Gly14=
XM_011509916.2:c.42G=	XP_011508218.1:p.Gly14=
XM_011509917.3:c.42G=	XP_011508219.1:p.Gly14=
XM_011509918.3:c.42G=	XP_011508220.1:p.Gly14=
XM_011509919.3:c.42G=	XP_011508221.1:p.Gly14=
XR_921911.3:n.168G=
XR_921912.2:n.170G=
NM_003126.4:c.42G= MANE Select	NP_003117.2:p.Gly14=