Canonical Allele Identifier: CA1381532925
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262081C= , CM000665.2:g.87262081C= GRCh38
NC_000003.11:g.87311231C= , CM000665.1:g.87311231C= GRCh37
NC_000003.10:g.87393921C= NCBI36
NG_008225.2:g.19507G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.672G= ENSP00000342931.3:p.Glu224=
ENST00000350375.7:c.594G= MANE Select ENSP00000263781.2:p.Glu198=
ENST00000344265.7:c.672G= ENSP00000342931.3:p.Glu224=
ENST00000350375.6:c.594G= ENSP00000263781.2:p.Glu198=
ENST00000560656.1:c.440-1977G= ENSP00000452610.1:n.440-1977G=
ENST00000561167.5:c.369G= ENSP00000454072.1:p.Glu123=
NM_000306.3:c.594G= NP_000297.1:p.Glu198=
NM_001122757.2:c.672G= NP_001116229.1:p.Glu224=
NM_000306.4:c.594G= MANE Select NP_000297.1:p.Glu198=
NM_001122757.3:c.672G= NP_001116229.1:p.Glu224=