Canonical Allele Identifier: CA1201546695

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158636763T= , CM000663.2:g.158636763T=	GRCh38
NC_000001.10:g.158606553T= , CM000663.1:g.158606553T=	GRCh37
NC_000001.9:g.156873177T=	NCBI36
NG_011474.1:g.54954A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.5190-2A= MANE Select	ENSP00000495214.1:n.5190-2A=
ENST00000368147.8:c.5190-2A=	ENSP00000357129.4:n.5190-2A=
ENST00000614909.4:c.5190-2A=	ENSP00000482595.1:n.5190-2A=
NM_003126.2:c.5190-2A=	NP_003117.2:n.5190-2A=
XM_011509916.1:c.5190-2A=	XP_011508218.1:n.5190-2A=
XM_011509917.1:c.5190-2A=	XP_011508219.1:n.5190-2A=
XM_011509918.1:c.5190-2A=	XP_011508220.1:n.5190-2A=
XM_011509919.1:c.4981-2A=	XP_011508221.1:n.4981-2A=
XR_921911.1:n.5303-2A=
NM_003126.3:c.5190-2A=	NP_003117.2:n.5190-2A=
XM_011509916.2:c.5190-2A=	XP_011508218.1:n.5190-2A=
XM_011509917.3:c.5190-2A=	XP_011508219.1:n.5190-2A=
XM_011509918.3:c.5190-2A=	XP_011508220.1:n.5190-2A=
XM_011509919.3:c.4981-2A=	XP_011508221.1:n.4981-2A=
XR_921911.3:n.5316-2A=
NM_003126.4:c.5190-2A= MANE Select	NP_003117.2:n.5190-2A=