Canonical Allele Identifier: CA343026730

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158655025C>T (hg19) ; chr1:g.158685235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685235C>T , CM000663.2:g.158685235C>T	GRCh38
NC_000001.10:g.158655025C>T , CM000663.1:g.158655025C>T	GRCh37
NC_000001.9:g.156921649C>T	NCBI36
NG_011474.1:g.6482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.137G>A MANE Select	ENSP00000495214.1:p.Gly46Asp
ENST00000368147.8:c.137G>A	ENSP00000357129.4:p.Gly46Asp
ENST00000467387.1:c.132+5G>A	ENSP00000476485.1:n.132+5G>A
ENST00000614909.4:c.137G>A	ENSP00000482595.1:p.Gly46Asp
NM_003126.2:c.137G>A	NP_003117.2:p.Gly46Asp
XM_011509916.1:c.137G>A	XP_011508218.1:p.Gly46Asp
XM_011509917.1:c.137G>A	XP_011508219.1:p.Gly46Asp
XM_011509918.1:c.137G>A	XP_011508220.1:p.Gly46Asp
XM_011509919.1:c.137G>A	XP_011508221.1:p.Gly46Asp
XR_921911.1:n.250G>A
XR_921912.1:n.255G>A
NM_003126.3:c.137G>A	NP_003117.2:p.Gly46Asp
XM_011509916.2:c.137G>A	XP_011508218.1:p.Gly46Asp
XM_011509917.3:c.137G>A	XP_011508219.1:p.Gly46Asp
XM_011509918.3:c.137G>A	XP_011508220.1:p.Gly46Asp
XM_011509919.3:c.137G>A	XP_011508221.1:p.Gly46Asp
XR_921911.3:n.263G>A
XR_921912.2:n.265G>A
NM_003126.4:c.137G>A MANE Select	NP_003117.2:p.Gly46Asp