Canonical Allele Identifier: CA1201556113

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158656669A= , CM000663.2:g.158656669A=	GRCh38
NC_000001.10:g.158626459A= , CM000663.1:g.158626459A=	GRCh37
NC_000001.9:g.156893083A=	NCBI36
NG_011474.1:g.35048T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003126.4:c.2806-13T= MANE Select	NP_003117.2:n.2806-13T=
ENST00000643759.2:c.2806-13T= MANE Select	ENSP00000495214.1:n.2806-13T=
NM_003126.2:c.2806-13T=	NP_003117.2:n.2806-13T=
NM_003126.3:c.2806-13T=	NP_003117.2:n.2806-13T=
ENST00000368147.8:c.2806-13T=	ENSP00000357129.4:n.2806-13T=
ENST00000614909.4:c.2806-13T=	ENSP00000482595.1:n.2806-13T=
ENST00000647256.1:n.406-13T=
XM_011509916.1:c.2806-13T=	XP_011508218.1:n.2806-13T=
XM_011509916.2:c.2806-13T=	XP_011508218.1:n.2806-13T=
XM_011509917.1:c.2806-13T=	XP_011508219.1:n.2806-13T=
XM_011509917.3:c.2806-13T=	XP_011508219.1:n.2806-13T=
XM_011509918.1:c.2806-13T=	XP_011508220.1:n.2806-13T=
XM_011509918.3:c.2806-13T=	XP_011508220.1:n.2806-13T=
XM_011509919.1:c.2806-13T=	XP_011508221.1:n.2806-13T=
XM_011509919.3:c.2806-13T=	XP_011508221.1:n.2806-13T=
XR_921911.1:n.2919-13T=
XR_921911.3:n.2932-13T=
XR_921912.1:n.2924-13T=
XR_921912.2:n.2934-13T=