Canonical Allele Identifier: CA343026878

Gene: SPTA1

Linked Data

• gnomAD v4: 1-158685306-T-G
• MyVariant Identifiers: chr1:g.158655096T>G (hg19) ; chr1:g.158685306T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685306T>G , CM000663.2:g.158685306T>G	GRCh38
NC_000001.10:g.158655096T>G , CM000663.1:g.158655096T>G	GRCh37
NC_000001.9:g.156921720T>G	NCBI36
NG_011474.1:g.6411A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.66A>C MANE Select	ENSP00000495214.1:p.Glu22Asp
ENST00000368147.8:c.66A>C	ENSP00000357129.4:p.Glu22Asp
ENST00000467387.1:c.66A>C	ENSP00000476485.1:p.Glu22Asp
ENST00000614909.4:c.66A>C	ENSP00000482595.1:p.Glu22Asp
NM_003126.2:c.66A>C	NP_003117.2:p.Glu22Asp
XM_011509916.1:c.66A>C	XP_011508218.1:p.Glu22Asp
XM_011509917.1:c.66A>C	XP_011508219.1:p.Glu22Asp
XM_011509918.1:c.66A>C	XP_011508220.1:p.Glu22Asp
XM_011509919.1:c.66A>C	XP_011508221.1:p.Glu22Asp
XR_921911.1:n.179A>C
XR_921912.1:n.184A>C
NM_003126.3:c.66A>C	NP_003117.2:p.Glu22Asp
XM_011509916.2:c.66A>C	XP_011508218.1:p.Glu22Asp
XM_011509917.3:c.66A>C	XP_011508219.1:p.Glu22Asp
XM_011509918.3:c.66A>C	XP_011508220.1:p.Glu22Asp
XM_011509919.3:c.66A>C	XP_011508221.1:p.Glu22Asp
XR_921911.3:n.192A>C
XR_921912.2:n.194A>C
NM_003126.4:c.66A>C MANE Select	NP_003117.2:p.Glu22Asp