Canonical Allele Identifier: CA353698199
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260009T>A , CM000665.2:g.87260009T>A GRCh38
NC_000003.11:g.87309159T>A , CM000665.1:g.87309159T>A GRCh37
NC_000003.10:g.87391849T>A NCBI36
NG_008225.2:g.21579A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.839A>T ENSP00000342931.3:p.Glu280Val
ENST00000350375.7:c.761A>T MANE Select ENSP00000263781.2:p.Glu254Val
ENST00000344265.7:c.839A>T ENSP00000342931.3:p.Glu280Val
ENST00000350375.6:c.761A>T ENSP00000263781.2:p.Glu254Val
ENST00000560656.1:c.535A>T ENSP00000452610.1:n.535A>T
ENST00000561167.5:c.536A>T ENSP00000454072.1:p.Glu179Val
NM_000306.3:c.761A>T NP_000297.1:p.Glu254Val
NM_001122757.2:c.839A>T NP_001116229.1:p.Glu280Val
NM_000306.4:c.761A>T MANE Select NP_000297.1:p.Glu254Val
NM_001122757.3:c.839A>T NP_001116229.1:p.Glu280Val