Canonical Allele Identifier: CA421301417

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158654979A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685189A>G , CM000663.2:g.158685189A>G	GRCh38
NC_000001.10:g.158654979A>G , CM000663.1:g.158654979A>G	GRCh37
NC_000001.9:g.156921603A>G	NCBI36
NG_011474.1:g.6528T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000643759.2:c.183T>C MANE Select	ENSP00000495214.1:p.Asp61=
ENST00000368147.8:c.183T>C	ENSP00000357129.4:p.Asp61=
ENST00000467387.1:c.132+51T>C	ENSP00000476485.1:n.132+51T>C
ENST00000614909.4:c.183T>C	ENSP00000482595.1:p.Asp61=
NM_003126.2:c.183T>C	NP_003117.2:p.Asp61=
XM_011509916.1:c.183T>C	XP_011508218.1:p.Asp61=
XM_011509917.1:c.183T>C	XP_011508219.1:p.Asp61=
XM_011509918.1:c.183T>C	XP_011508220.1:p.Asp61=
XM_011509919.1:c.183T>C	XP_011508221.1:p.Asp61=
XR_921911.1:n.296T>C
XR_921912.1:n.301T>C
NM_003126.3:c.183T>C	NP_003117.2:p.Asp61=
XM_011509916.2:c.183T>C	XP_011508218.1:p.Asp61=
XM_011509917.3:c.183T>C	XP_011508219.1:p.Asp61=
XM_011509918.3:c.183T>C	XP_011508220.1:p.Asp61=
XM_011509919.3:c.183T>C	XP_011508221.1:p.Asp61=
XR_921911.3:n.309T>C
XR_921912.2:n.311T>C
NM_003126.4:c.183T>C MANE Select	NP_003117.2:p.Asp61=