Canonical Allele Identifier: CA1141300179

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612847C= , CM000663.2:g.158612847C=	GRCh38
NC_000001.10:g.158582637C= , CM000663.1:g.158582637C=	GRCh37
NC_000001.9:g.156849261C=	NCBI36
NG_011474.1:g.78870G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7104G= MANE Select	ENSP00000495214.1:p.Lys2368=
ENST00000368147.8:c.7104G=	ENSP00000357129.4:p.Lys2368=
ENST00000481212.5:n.545G=
ENST00000498708.1:n.536G=
ENST00000614909.4:c.7104G=	ENSP00000482595.1:p.Lys2368=
NM_003126.2:c.7104G=	NP_003117.2:p.Lys2368=
XM_011509916.1:c.7104G=	XP_011508218.1:p.Lys2368=
XM_011509917.1:c.7086G=	XP_011508219.1:p.Lys2362=
NM_003126.3:c.7104G=	NP_003117.2:p.Lys2368=
XM_011509916.2:c.7104G=	XP_011508218.1:p.Lys2368=
XM_011509917.3:c.7086G=	XP_011508219.1:p.Lys2362=
NM_003126.4:c.7104G= MANE Select	NP_003117.2:p.Lys2368=