Canonical Allele Identifier: CA343020616

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158650425G>T (hg19) ; chr1:g.158680635G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158680635G>T , CM000663.2:g.158680635G>T	GRCh38
NC_000001.10:g.158650425G>T , CM000663.1:g.158650425G>T	GRCh37
NC_000001.9:g.156917049G>T	NCBI36
NG_011474.1:g.11082C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.626C>A MANE Select	ENSP00000495214.1:p.Ala209Asp
ENST00000368147.8:c.626C>A	ENSP00000357129.4:p.Ala209Asp
ENST00000467387.1:c.133-2101C>A	ENSP00000476485.1:n.133-2101C>A
ENST00000614909.4:c.626C>A	ENSP00000482595.1:p.Ala209Asp
NM_003126.2:c.626C>A	NP_003117.2:p.Ala209Asp
XM_011509916.1:c.626C>A	XP_011508218.1:p.Ala209Asp
XM_011509917.1:c.626C>A	XP_011508219.1:p.Ala209Asp
XM_011509918.1:c.626C>A	XP_011508220.1:p.Ala209Asp
XM_011509919.1:c.626C>A	XP_011508221.1:p.Ala209Asp
XR_921911.1:n.739C>A
XR_921912.1:n.744C>A
NM_003126.3:c.626C>A	NP_003117.2:p.Ala209Asp
XM_011509916.2:c.626C>A	XP_011508218.1:p.Ala209Asp
XM_011509917.3:c.626C>A	XP_011508219.1:p.Ala209Asp
XM_011509918.3:c.626C>A	XP_011508220.1:p.Ala209Asp
XM_011509919.3:c.626C>A	XP_011508221.1:p.Ala209Asp
XR_921911.3:n.752C>A
XR_921912.2:n.754C>A
NM_003126.4:c.626C>A MANE Select	NP_003117.2:p.Ala209Asp