Canonical Allele Identifier: CA353692758
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262100T>G , CM000665.2:g.87262100T>G GRCh38
NC_000003.11:g.87311250T>G , CM000665.1:g.87311250T>G GRCh37
NC_000003.10:g.87393940T>G NCBI36
NG_008225.2:g.19488A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.653A>C ENSP00000342931.3:p.Lys218Thr
ENST00000350375.7:c.575A>C MANE Select ENSP00000263781.2:p.Lys192Thr
ENST00000344265.7:c.653A>C ENSP00000342931.3:p.Lys218Thr
ENST00000350375.6:c.575A>C ENSP00000263781.2:p.Lys192Thr
ENST00000560656.1:c.440-1996A>C ENSP00000452610.1:n.440-1996A>C
ENST00000561167.5:c.350A>C ENSP00000454072.1:p.Lys117Thr
NM_000306.3:c.575A>C NP_000297.1:p.Lys192Thr
NM_001122757.2:c.653A>C NP_001116229.1:p.Lys218Thr
NM_000306.4:c.575A>C MANE Select NP_000297.1:p.Lys192Thr
NM_001122757.3:c.653A>C NP_001116229.1:p.Lys218Thr