Canonical Allele Identifier: CA353693824
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264365G>T , CM000665.2:g.87264365G>T GRCh38
NC_000003.11:g.87313515G>T , CM000665.1:g.87313515G>T GRCh37
NC_000003.10:g.87396205G>T NCBI36
NG_008225.2:g.17223C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.440C>A ENSP00000342931.3:p.Pro147Gln
ENST00000350375.7:c.362C>A MANE Select ENSP00000263781.2:p.Pro121Gln
ENST00000344265.7:c.440C>A ENSP00000342931.3:p.Pro147Gln
ENST00000350375.6:c.362C>A ENSP00000263781.2:p.Pro121Gln
ENST00000560656.1:c.362C>A ENSP00000452610.1:p.Pro121Gln
ENST00000561167.5:c.215-2130C>A ENSP00000454072.1:n.215-2130C>A
NM_000306.3:c.362C>A NP_000297.1:p.Pro121Gln
NM_001122757.2:c.440C>A NP_001116229.1:p.Pro147Gln
NM_000306.4:c.362C>A MANE Select NP_000297.1:p.Pro121Gln
NM_001122757.3:c.440C>A NP_001116229.1:p.Pro147Gln