Canonical Allele Identifier: CA353693692
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1316739446
gnomAD v2: 3-87313486-C-T
gnomAD v4: 3-87264336-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264336C>T , CM000665.2:g.87264336C>T GRCh38
NC_000003.11:g.87313486C>T , CM000665.1:g.87313486C>T GRCh37
NC_000003.10:g.87396176C>T NCBI36
NG_008225.2:g.17252G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.469G>A ENSP00000342931.3:p.Glu157Lys
ENST00000350375.7:c.391G>A MANE Select ENSP00000263781.2:p.Glu131Lys
ENST00000344265.7:c.469G>A ENSP00000342931.3:p.Glu157Lys
ENST00000350375.6:c.391G>A ENSP00000263781.2:p.Glu131Lys
ENST00000560656.1:c.391G>A ENSP00000452610.1:p.Glu131Lys
ENST00000561167.5:c.215-2101G>A ENSP00000454072.1:n.215-2101G>A
NM_000306.3:c.391G>A NP_000297.1:p.Glu131Lys
NM_001122757.2:c.469G>A NP_001116229.1:p.Glu157Lys
NM_000306.4:c.391G>A MANE Select NP_000297.1:p.Glu131Lys
NM_001122757.3:c.469G>A NP_001116229.1:p.Glu157Lys