Canonical Allele Identifier: CA1201536941

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612938T= , CM000663.2:g.158612938T=	GRCh38
NC_000001.10:g.158582728T= , CM000663.1:g.158582728T=	GRCh37
NC_000001.9:g.156849352T=	NCBI36
NG_011474.1:g.78779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7013A= MANE Select	ENSP00000495214.1:p.Asp2338=
ENST00000368147.8:c.7013A=	ENSP00000357129.4:p.Asp2338=
ENST00000481212.5:n.454A=
ENST00000498708.1:n.445A=
ENST00000614909.4:c.7013A=	ENSP00000482595.1:p.Asp2338=
NM_003126.2:c.7013A=	NP_003117.2:p.Asp2338=
XM_011509916.1:c.7013A=	XP_011508218.1:p.Asp2338=
XM_011509917.1:c.6995A=	XP_011508219.1:p.Asp2332=
NM_003126.3:c.7013A=	NP_003117.2:p.Asp2338=
XM_011509916.2:c.7013A=	XP_011508218.1:p.Asp2338=
XM_011509917.3:c.6995A=	XP_011508219.1:p.Asp2332=
NM_003126.4:c.7013A= MANE Select	NP_003117.2:p.Asp2338=