Canonical Allele Identifier: CA343011189

Gene: SPTA1

Linked Data

• dbSNP Id: rs772533002
• MyVariant Identifiers: chr1:g.158582643C>A (hg19) ; chr1:g.158612853C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612853C>A , CM000663.2:g.158612853C>A	GRCh38
NC_000001.10:g.158582643C>A , CM000663.1:g.158582643C>A	GRCh37
NC_000001.9:g.156849267C>A	NCBI36
NG_011474.1:g.78864G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7098G>T MANE Select	ENSP00000495214.1:p.Glu2366Asp
ENST00000368147.8:c.7098G>T	ENSP00000357129.4:p.Glu2366Asp
ENST00000481212.5:n.539G>T
ENST00000498708.1:n.530G>T
ENST00000614909.4:c.7098G>T	ENSP00000482595.1:p.Glu2366Asp
NM_003126.2:c.7098G>T	NP_003117.2:p.Glu2366Asp
XM_011509916.1:c.7098G>T	XP_011508218.1:p.Glu2366Asp
XM_011509917.1:c.7080G>T	XP_011508219.1:p.Glu2360Asp
NM_003126.3:c.7098G>T	NP_003117.2:p.Glu2366Asp
XM_011509916.2:c.7098G>T	XP_011508218.1:p.Glu2366Asp
XM_011509917.3:c.7080G>T	XP_011508219.1:p.Glu2360Asp
NM_003126.4:c.7098G>T MANE Select	NP_003117.2:p.Glu2366Asp