Canonical Allele Identifier: CA2757123229
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259976del , CM000665.2:g.87259976del GRCh38
NC_000003.11:g.87309126del , CM000665.1:g.87309126del GRCh37
NC_000003.10:g.87391816del NCBI36
NG_008225.2:g.21613del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.873del ENSP00000342931.3:p.Arg292GlyfsTer7
ENST00000350375.7:c.795del MANE Select ENSP00000263781.2:p.Arg266GlyfsTer7
ENST00000344265.7:c.873del ENSP00000342931.3:p.Arg292GlyfsTer7
ENST00000350375.6:c.795del ENSP00000263781.2:p.Arg266GlyfsTer7
ENST00000560656.1:c.569del ENSP00000452610.1:n.569del
ENST00000561167.5:c.570del ENSP00000454072.1:p.Arg191GlyfsTer7
NM_000306.3:c.795del NP_000297.1:p.Arg266GlyfsTer7
NM_001122757.2:c.873del NP_001116229.1:p.Arg292GlyfsTer7
NM_000306.4:c.795del MANE Select NP_000297.1:p.Arg266GlyfsTer7
NM_001122757.3:c.873del NP_001116229.1:p.Arg292GlyfsTer7