Canonical Allele Identifier: CA353692780
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262110T>C , CM000665.2:g.87262110T>C GRCh38
NC_000003.11:g.87311260T>C , CM000665.1:g.87311260T>C GRCh37
NC_000003.10:g.87393950T>C NCBI36
NG_008225.2:g.19478A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.643A>G ENSP00000342931.3:p.Ile215Val
ENST00000350375.7:c.565A>G MANE Select ENSP00000263781.2:p.Ile189Val
ENST00000344265.7:c.643A>G ENSP00000342931.3:p.Ile215Val
ENST00000350375.6:c.565A>G ENSP00000263781.2:p.Ile189Val
ENST00000560656.1:c.440-2006A>G ENSP00000452610.1:n.440-2006A>G
ENST00000561167.5:c.340A>G ENSP00000454072.1:p.Ile114Val
NM_000306.3:c.565A>G NP_000297.1:p.Ile189Val
NM_001122757.2:c.643A>G NP_001116229.1:p.Ile215Val
NM_000306.4:c.565A>G MANE Select NP_000297.1:p.Ile189Val
NM_001122757.3:c.643A>G NP_001116229.1:p.Ile215Val