Canonical Allele Identifier: CA421213019

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158582736T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612946T>C , CM000663.2:g.158612946T>C	GRCh38
NC_000001.10:g.158582736T>C , CM000663.1:g.158582736T>C	GRCh37
NC_000001.9:g.156849360T>C	NCBI36
NG_011474.1:g.78771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7005A>G MANE Select	ENSP00000495214.1:p.Ser2335=
ENST00000368147.8:c.7005A>G	ENSP00000357129.4:p.Ser2335=
ENST00000481212.5:n.446A>G
ENST00000498708.1:n.437A>G
ENST00000614909.4:c.7005A>G	ENSP00000482595.1:p.Ser2335=
NM_003126.2:c.7005A>G	NP_003117.2:p.Ser2335=
XM_011509916.1:c.7005A>G	XP_011508218.1:p.Ser2335=
XM_011509917.1:c.6987A>G	XP_011508219.1:p.Ser2329=
NM_003126.3:c.7005A>G	NP_003117.2:p.Ser2335=
XM_011509916.2:c.7005A>G	XP_011508218.1:p.Ser2335=
XM_011509917.3:c.6987A>G	XP_011508219.1:p.Ser2329=
NM_003126.4:c.7005A>G MANE Select	NP_003117.2:p.Ser2335=