Canonical Allele Identifier: CA434627069
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87313499A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264349A>T , CM000665.2:g.87264349A>T GRCh38
NC_000003.11:g.87313499A>T , CM000665.1:g.87313499A>T GRCh37
NC_000003.10:g.87396189A>T NCBI36
NG_008225.2:g.17239T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.456T>A ENSP00000342931.3:p.Ser152=
ENST00000350375.7:c.378T>A MANE Select ENSP00000263781.2:p.Ser126=
ENST00000344265.7:c.456T>A ENSP00000342931.3:p.Ser152=
ENST00000350375.6:c.378T>A ENSP00000263781.2:p.Ser126=
ENST00000560656.1:c.378T>A ENSP00000452610.1:p.Ser126=
ENST00000561167.5:c.215-2114T>A ENSP00000454072.1:n.215-2114T>A
NM_000306.3:c.378T>A NP_000297.1:p.Ser126=
NM_001122757.2:c.456T>A NP_001116229.1:p.Ser152=
NM_000306.4:c.378T>A MANE Select NP_000297.1:p.Ser126=
NM_001122757.3:c.456T>A NP_001116229.1:p.Ser152=