Canonical Allele Identifier: CA1146990838
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612732T= , CM000663.2:g.158612732T= GRCh38
NC_000001.10:g.158582522T= , CM000663.1:g.158582522T= GRCh37
NC_000001.9:g.156849146T= NCBI36
NG_011474.1:g.78985A=

Transcript Alleles

HGVS Amino-acid change
ENST00000643759.2:c.7134+85A= MANE Select ENSP00000495214.1:n.7134+85A=
ENST00000368147.8:c.7134+85A= ENSP00000357129.4:n.7134+85A=
ENST00000614909.4:c.7134+85A= ENSP00000482595.1:n.7134+85A=
NM_003126.2:c.7134+85A= NP_003117.2:n.7134+85A=
XM_011509916.1:c.7134+85A= XP_011508218.1:n.7134+85A=
XM_011509917.1:c.7116+85A= XP_011508219.1:n.7116+85A=
NM_003126.3:c.7134+85A= NP_003117.2:n.7134+85A=
XM_011509916.2:c.7134+85A= XP_011508218.1:n.7134+85A=
XM_011509917.3:c.7116+85A= XP_011508219.1:n.7116+85A=
NM_003126.4:c.7134+85A= MANE Select NP_003117.2:n.7134+85A=