Canonical Allele Identifier: CA353693672
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264332A>C , CM000665.2:g.87264332A>C GRCh38
NC_000003.11:g.87313482A>C , CM000665.1:g.87313482A>C GRCh37
NC_000003.10:g.87396172A>C NCBI36
NG_008225.2:g.17256T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.473T>G ENSP00000342931.3:p.Leu158Arg
ENST00000350375.7:c.395T>G MANE Select ENSP00000263781.2:p.Leu132Arg
ENST00000344265.7:c.473T>G ENSP00000342931.3:p.Leu158Arg
ENST00000350375.6:c.395T>G ENSP00000263781.2:p.Leu132Arg
ENST00000560656.1:c.395T>G ENSP00000452610.1:p.Leu132Arg
ENST00000561167.5:c.215-2097T>G ENSP00000454072.1:n.215-2097T>G
NM_000306.3:c.395T>G NP_000297.1:p.Leu132Arg
NM_001122757.2:c.473T>G NP_001116229.1:p.Leu158Arg
NM_000306.4:c.395T>G MANE Select NP_000297.1:p.Leu132Arg
NM_001122757.3:c.473T>G NP_001116229.1:p.Leu158Arg