Canonical Allele Identifier: CA1201568182

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685310G= , CM000663.2:g.158685310G=	GRCh38
NC_000001.10:g.158655100G= , CM000663.1:g.158655100G=	GRCh37
NC_000001.9:g.156921724G=	NCBI36
NG_011474.1:g.6407C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.62C= MANE Select	ENSP00000495214.1:p.Ala21=
ENST00000368147.8:c.62C=	ENSP00000357129.4:p.Ala21=
ENST00000467387.1:c.62C=	ENSP00000476485.1:p.Ala21=
ENST00000614909.4:c.62C=	ENSP00000482595.1:p.Ala21=
NM_003126.2:c.62C=	NP_003117.2:p.Ala21=
XM_011509916.1:c.62C=	XP_011508218.1:p.Ala21=
XM_011509917.1:c.62C=	XP_011508219.1:p.Ala21=
XM_011509918.1:c.62C=	XP_011508220.1:p.Ala21=
XM_011509919.1:c.62C=	XP_011508221.1:p.Ala21=
XR_921911.1:n.175C=
XR_921912.1:n.180C=
NM_003126.3:c.62C=	NP_003117.2:p.Ala21=
XM_011509916.2:c.62C=	XP_011508218.1:p.Ala21=
XM_011509917.3:c.62C=	XP_011508219.1:p.Ala21=
XM_011509918.3:c.62C=	XP_011508220.1:p.Ala21=
XM_011509919.3:c.62C=	XP_011508221.1:p.Ala21=
XR_921911.3:n.188C=
XR_921912.2:n.190C=
NM_003126.4:c.62C= MANE Select	NP_003117.2:p.Ala21=