Canonical Allele Identifier: CA343011127

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158582626G>C (hg19) ; chr1:g.158612836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612836G>C , CM000663.2:g.158612836G>C	GRCh38
NC_000001.10:g.158582626G>C , CM000663.1:g.158582626G>C	GRCh37
NC_000001.9:g.156849250G>C	NCBI36
NG_011474.1:g.78881C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7115C>G MANE Select	ENSP00000495214.1:p.Thr2372Ser
ENST00000368147.8:c.7115C>G	ENSP00000357129.4:p.Thr2372Ser
ENST00000481212.5:n.556C>G
ENST00000498708.1:n.547C>G
ENST00000614909.4:c.7115C>G	ENSP00000482595.1:p.Thr2372Ser
NM_003126.2:c.7115C>G	NP_003117.2:p.Thr2372Ser
XM_011509916.1:c.7115C>G	XP_011508218.1:p.Thr2372Ser
XM_011509917.1:c.7097C>G	XP_011508219.1:p.Thr2366Ser
NM_003126.3:c.7115C>G	NP_003117.2:p.Thr2372Ser
XM_011509916.2:c.7115C>G	XP_011508218.1:p.Thr2372Ser
XM_011509917.3:c.7097C>G	XP_011508219.1:p.Thr2366Ser
NM_003126.4:c.7115C>G MANE Select	NP_003117.2:p.Thr2372Ser