Canonical Allele Identifier: CA1201536959

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612975G= , CM000663.2:g.158612975G=	GRCh38
NC_000001.10:g.158582765G= , CM000663.1:g.158582765G=	GRCh37
NC_000001.9:g.156849389G=	NCBI36
NG_011474.1:g.78742C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.6990-14C= MANE Select	ENSP00000495214.1:n.6990-14C=
ENST00000368147.8:c.6990-14C=	ENSP00000357129.4:n.6990-14C=
ENST00000481212.5:n.431-14C=
ENST00000498708.1:n.422-14C=
ENST00000614909.4:c.6990-14C=	ENSP00000482595.1:n.6990-14C=
NM_003126.2:c.6990-14C=	NP_003117.2:n.6990-14C=
XM_011509916.1:c.6990-14C=	XP_011508218.1:n.6990-14C=
XM_011509917.1:c.6972-14C=	XP_011508219.1:n.6972-14C=
NM_003126.3:c.6990-14C=	NP_003117.2:n.6990-14C=
XM_011509916.2:c.6990-14C=	XP_011508218.1:n.6990-14C=
XM_011509917.3:c.6972-14C=	XP_011508219.1:n.6972-14C=
NM_003126.4:c.6990-14C= MANE Select	NP_003117.2:n.6990-14C=