Canonical Allele Identifier: CA353692776
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262109A>G , CM000665.2:g.87262109A>G GRCh38
NC_000003.11:g.87311259A>G , CM000665.1:g.87311259A>G GRCh37
NC_000003.10:g.87393949A>G NCBI36
NG_008225.2:g.19479T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.644T>C ENSP00000342931.3:p.Ile215Thr
ENST00000350375.7:c.566T>C MANE Select ENSP00000263781.2:p.Ile189Thr
ENST00000344265.7:c.644T>C ENSP00000342931.3:p.Ile215Thr
ENST00000350375.6:c.566T>C ENSP00000263781.2:p.Ile189Thr
ENST00000560656.1:c.440-2005T>C ENSP00000452610.1:n.440-2005T>C
ENST00000561167.5:c.341T>C ENSP00000454072.1:p.Ile114Thr
NM_000306.3:c.566T>C NP_000297.1:p.Ile189Thr
NM_001122757.2:c.644T>C NP_001116229.1:p.Ile215Thr
NM_000306.4:c.566T>C MANE Select NP_000297.1:p.Ile189Thr
NM_001122757.3:c.644T>C NP_001116229.1:p.Ile215Thr