Canonical Allele Identifier: CA1381564007
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259966T= , CM000665.2:g.87259966T= GRCh38
NC_000003.11:g.87309116T= , CM000665.1:g.87309116T= GRCh37
NC_000003.10:g.87391806T= NCBI36
NG_008225.2:g.21622A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.882A= ENSP00000342931.3:p.Arg294=
ENST00000350375.7:c.804A= MANE Select ENSP00000263781.2:p.Arg268=
ENST00000344265.7:c.882A= ENSP00000342931.3:p.Arg294=
ENST00000350375.6:c.804A= ENSP00000263781.2:p.Arg268=
ENST00000560656.1:c.578A= ENSP00000452610.1:n.578A=
ENST00000561167.5:c.579A= ENSP00000454072.1:p.Arg193=
NM_000306.3:c.804A= NP_000297.1:p.Arg268=
NM_001122757.2:c.882A= NP_001116229.1:p.Arg294=
NM_000306.4:c.804A= MANE Select NP_000297.1:p.Arg268=
NM_001122757.3:c.882A= NP_001116229.1:p.Arg294=