Canonical Allele Identifier: CA434579440
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259975-C-T
MyVariant Identifiers: chr3:g.87309125C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259975C>T , CM000665.2:g.87259975C>T GRCh38
NC_000003.11:g.87309125C>T , CM000665.1:g.87309125C>T GRCh37
NC_000003.10:g.87391815C>T NCBI36
NG_008225.2:g.21613G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.873G>A ENSP00000342931.3:p.Arg291=
ENST00000350375.7:c.795G>A MANE Select ENSP00000263781.2:p.Arg265=
ENST00000344265.7:c.873G>A ENSP00000342931.3:p.Arg291=
ENST00000350375.6:c.795G>A ENSP00000263781.2:p.Arg265=
ENST00000560656.1:c.569G>A ENSP00000452610.1:n.569G>A
ENST00000561167.5:c.570G>A ENSP00000454072.1:p.Arg190=
NM_000306.3:c.795G>A NP_000297.1:p.Arg265=
NM_001122757.2:c.873G>A NP_001116229.1:p.Arg291=
NM_000306.4:c.795G>A MANE Select NP_000297.1:p.Arg265=
NM_001122757.3:c.873G>A NP_001116229.1:p.Arg291=