Canonical Allele Identifier: CA343011693

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158582726A>C (hg19) ; chr1:g.158612936A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612936A>C , CM000663.2:g.158612936A>C	GRCh38
NC_000001.10:g.158582726A>C , CM000663.1:g.158582726A>C	GRCh37
NC_000001.9:g.156849350A>C	NCBI36
NG_011474.1:g.78781T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7015T>G MANE Select	ENSP00000495214.1:p.Tyr2339Asp
ENST00000368147.8:c.7015T>G	ENSP00000357129.4:p.Tyr2339Asp
ENST00000481212.5:n.456T>G
ENST00000498708.1:n.447T>G
ENST00000614909.4:c.7015T>G	ENSP00000482595.1:p.Tyr2339Asp
NM_003126.2:c.7015T>G	NP_003117.2:p.Tyr2339Asp
XM_011509916.1:c.7015T>G	XP_011508218.1:p.Tyr2339Asp
XM_011509917.1:c.6997T>G	XP_011508219.1:p.Tyr2333Asp
NM_003126.3:c.7015T>G	NP_003117.2:p.Tyr2339Asp
XM_011509916.2:c.7015T>G	XP_011508218.1:p.Tyr2339Asp
XM_011509917.3:c.6997T>G	XP_011508219.1:p.Tyr2333Asp
NM_003126.4:c.7015T>G MANE Select	NP_003117.2:p.Tyr2339Asp