Canonical Allele Identifier: CA1201568140
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158685192T= , CM000663.2:g.158685192T= GRCh38
NC_000001.10:g.158654982T= , CM000663.1:g.158654982T= GRCh37
NC_000001.9:g.156921606T= NCBI36
NG_011474.1:g.6525A=

Transcript Alleles

HGVS Amino-acid change
ENST00000643759.2:c.180A= MANE Select ENSP00000495214.1:p.Arg60=
ENST00000368147.8:c.180A= ENSP00000357129.4:p.Arg60=
ENST00000467387.1:c.132+48A= ENSP00000476485.1:n.132+48A=
ENST00000614909.4:c.180A= ENSP00000482595.1:p.Arg60=
NM_003126.2:c.180A= NP_003117.2:p.Arg60=
XM_011509916.1:c.180A= XP_011508218.1:p.Arg60=
XM_011509917.1:c.180A= XP_011508219.1:p.Arg60=
XM_011509918.1:c.180A= XP_011508220.1:p.Arg60=
XM_011509919.1:c.180A= XP_011508221.1:p.Arg60=
XR_921911.1:n.293A=
XR_921912.1:n.298A=
NM_003126.3:c.180A= NP_003117.2:p.Arg60=
XM_011509916.2:c.180A= XP_011508218.1:p.Arg60=
XM_011509917.3:c.180A= XP_011508219.1:p.Arg60=
XM_011509918.3:c.180A= XP_011508220.1:p.Arg60=
XM_011509919.3:c.180A= XP_011508221.1:p.Arg60=
XR_921911.3:n.306A=
XR_921912.2:n.308A=
NM_003126.4:c.180A= MANE Select NP_003117.2:p.Arg60=