Canonical Allele Identifier: CA1148271467

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612932G= , CM000663.2:g.158612932G=	GRCh38
NC_000001.10:g.158582722G= , CM000663.1:g.158582722G=	GRCh37
NC_000001.9:g.156849346G=	NCBI36
NG_011474.1:g.78785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7019C= MANE Select	ENSP00000495214.1:p.Thr2340=
ENST00000368147.8:c.7019C=	ENSP00000357129.4:p.Thr2340=
ENST00000481212.5:n.460C=
ENST00000498708.1:n.451C=
ENST00000614909.4:c.7019C=	ENSP00000482595.1:p.Thr2340=
NM_003126.2:c.7019C=	NP_003117.2:p.Thr2340=
XM_011509916.1:c.7019C=	XP_011508218.1:p.Thr2340=
XM_011509917.1:c.7001C=	XP_011508219.1:p.Thr2334=
NM_003126.3:c.7019C=	NP_003117.2:p.Thr2340=
XM_011509916.2:c.7019C=	XP_011508218.1:p.Thr2340=
XM_011509917.3:c.7001C=	XP_011508219.1:p.Thr2334=
NM_003126.4:c.7019C= MANE Select	NP_003117.2:p.Thr2340=