Canonical Allele Identifier: CA1381564021
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259977G= , CM000665.2:g.87259977G= GRCh38
NC_000003.11:g.87309127G= , CM000665.1:g.87309127G= GRCh37
NC_000003.10:g.87391817G= NCBI36
NG_008225.2:g.21611C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.871C= ENSP00000342931.3:p.Arg291=
ENST00000350375.7:c.793C= MANE Select ENSP00000263781.2:p.Arg265=
ENST00000344265.7:c.871C= ENSP00000342931.3:p.Arg291=
ENST00000350375.6:c.793C= ENSP00000263781.2:p.Arg265=
ENST00000560656.1:c.567C= ENSP00000452610.1:n.567C=
ENST00000561167.5:c.568C= ENSP00000454072.1:p.Arg190=
NM_000306.3:c.793C= NP_000297.1:p.Arg265=
NM_001122757.2:c.871C= NP_001116229.1:p.Arg291=
NM_000306.4:c.793C= MANE Select NP_000297.1:p.Arg265=
NM_001122757.3:c.871C= NP_001116229.1:p.Arg291=