Canonical Allele Identifier: CA353692779
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.643A>C ENSP00000342931.3:p.Ile215Leu
ENST00000350375.7:c.565A>C MANE Select ENSP00000263781.2:p.Ile189Leu
ENST00000344265.7:c.643A>C ENSP00000342931.3:p.Ile215Leu
ENST00000350375.6:c.565A>C ENSP00000263781.2:p.Ile189Leu
ENST00000560656.1:c.440-2006A>C ENSP00000452610.1:n.440-2006A>C
ENST00000561167.5:c.340A>C ENSP00000454072.1:p.Ile114Leu
NM_000306.3:c.565A>C NP_000297.1:p.Ile189Leu
NM_001122757.2:c.643A>C NP_001116229.1:p.Ile215Leu
NM_000306.4:c.565A>C MANE Select NP_000297.1:p.Ile189Leu
NM_001122757.3:c.643A>C NP_001116229.1:p.Ile215Leu