Canonical Allele Identifier: CA434627109
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87313544G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264394G>T , CM000665.2:g.87264394G>T GRCh38
NC_000003.11:g.87313544G>T , CM000665.1:g.87313544G>T GRCh37
NC_000003.10:g.87396234G>T NCBI36
NG_008225.2:g.17194C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.411C>A ENSP00000342931.3:p.Leu137=
ENST00000350375.7:c.333C>A MANE Select ENSP00000263781.2:p.Leu111=
ENST00000344265.7:c.411C>A ENSP00000342931.3:p.Leu137=
ENST00000350375.6:c.333C>A ENSP00000263781.2:p.Leu111=
ENST00000560656.1:c.333C>A ENSP00000452610.1:p.Leu111=
ENST00000561167.5:c.215-2159C>A ENSP00000454072.1:n.215-2159C>A
NM_000306.3:c.333C>A NP_000297.1:p.Leu111=
NM_001122757.2:c.411C>A NP_001116229.1:p.Leu137=
NM_000306.4:c.333C>A MANE Select NP_000297.1:p.Leu111=
NM_001122757.3:c.411C>A NP_001116229.1:p.Leu137=