Canonical Allele Identifier: CA343020447

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158650389G>A (hg19) ; chr1:g.158680599G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158680599G>A , CM000663.2:g.158680599G>A	GRCh38
NC_000001.10:g.158650389G>A , CM000663.1:g.158650389G>A	GRCh37
NC_000001.9:g.156917013G>A	NCBI36
NG_011474.1:g.11118C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.662C>T MANE Select	ENSP00000495214.1:p.Ala221Val
ENST00000368147.8:c.662C>T	ENSP00000357129.4:p.Ala221Val
ENST00000467387.1:c.133-2065C>T	ENSP00000476485.1:n.133-2065C>T
ENST00000614909.4:c.662C>T	ENSP00000482595.1:p.Ala221Val
NM_003126.2:c.662C>T	NP_003117.2:p.Ala221Val
XM_011509916.1:c.662C>T	XP_011508218.1:p.Ala221Val
XM_011509917.1:c.662C>T	XP_011508219.1:p.Ala221Val
XM_011509918.1:c.662C>T	XP_011508220.1:p.Ala221Val
XM_011509919.1:c.662C>T	XP_011508221.1:p.Ala221Val
XR_921911.1:n.775C>T
XR_921912.1:n.780C>T
NM_003126.3:c.662C>T	NP_003117.2:p.Ala221Val
XM_011509916.2:c.662C>T	XP_011508218.1:p.Ala221Val
XM_011509917.3:c.662C>T	XP_011508219.1:p.Ala221Val
XM_011509918.3:c.662C>T	XP_011508220.1:p.Ala221Val
XM_011509919.3:c.662C>T	XP_011508221.1:p.Ala221Val
XR_921911.3:n.788C>T
XR_921912.2:n.790C>T
NM_003126.4:c.662C>T MANE Select	NP_003117.2:p.Ala221Val