Canonical Allele Identifier: CA1201536908

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612819G= , CM000663.2:g.158612819G=	GRCh38
NC_000001.10:g.158582609G= , CM000663.1:g.158582609G=	GRCh37
NC_000001.9:g.156849233G=	NCBI36
NG_011474.1:g.78898C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7132C= MANE Select	ENSP00000495214.1:p.Gln2378=
ENST00000368147.8:c.7132C=	ENSP00000357129.4:p.Gln2378=
ENST00000481212.5:n.573C=
ENST00000498708.1:n.564C=
ENST00000614909.4:c.7132C=	ENSP00000482595.1:p.Gln2378=
NM_003126.2:c.7132C=	NP_003117.2:p.Gln2378=
XM_011509916.1:c.7132C=	XP_011508218.1:p.Gln2378=
XM_011509917.1:c.7114C=	XP_011508219.1:p.Gln2372=
NM_003126.3:c.7132C=	NP_003117.2:p.Gln2378=
XM_011509916.2:c.7132C=	XP_011508218.1:p.Gln2378=
XM_011509917.3:c.7114C=	XP_011508219.1:p.Gln2372=
NM_003126.4:c.7132C= MANE Select	NP_003117.2:p.Gln2378=