Canonical Allele Identifier: CA1381564012
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259969C= , CM000665.2:g.87259969C= GRCh38
NC_000003.11:g.87309119C= , CM000665.1:g.87309119C= GRCh37
NC_000003.10:g.87391809C= NCBI36
NG_008225.2:g.21619G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.879G= ENSP00000342931.3:p.Gln293=
ENST00000350375.7:c.801G= MANE Select ENSP00000263781.2:p.Gln267=
ENST00000344265.7:c.879G= ENSP00000342931.3:p.Gln293=
ENST00000350375.6:c.801G= ENSP00000263781.2:p.Gln267=
ENST00000560656.1:c.575G= ENSP00000452610.1:n.575G=
ENST00000561167.5:c.576G= ENSP00000454072.1:p.Gln192=
NM_000306.3:c.801G= NP_000297.1:p.Gln267=
NM_001122757.2:c.879G= NP_001116229.1:p.Gln293=
NM_000306.4:c.801G= MANE Select NP_000297.1:p.Gln267=
NM_001122757.3:c.879G= NP_001116229.1:p.Gln293=