Canonical Allele Identifier: CA434579443

Gene: POU1F1

Linked Data

• dbSNP Id: rs780359925
• COSMIC: COSM6026849 ; COSM6026850
• MyVariant Identifiers: chr3:g.87309127G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259977G>T , CM000665.2:g.87259977G>T	GRCh38
NC_000003.11:g.87309127G>T , CM000665.1:g.87309127G>T	GRCh37
NC_000003.10:g.87391817G>T	NCBI36
NG_008225.2:g.21611C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.871C>A	ENSP00000342931.3:p.Arg291=
ENST00000350375.7:c.793C>A MANE Select	ENSP00000263781.2:p.Arg265=
ENST00000344265.7:c.871C>A	ENSP00000342931.3:p.Arg291=
ENST00000350375.6:c.793C>A	ENSP00000263781.2:p.Arg265=
ENST00000560656.1:c.567C>A	ENSP00000452610.1:n.567C>A
ENST00000561167.5:c.568C>A	ENSP00000454072.1:p.Arg190=
NM_000306.3:c.793C>A	NP_000297.1:p.Arg265=
NM_001122757.2:c.871C>A	NP_001116229.1:p.Arg291=
NM_000306.4:c.793C>A MANE Select	NP_000297.1:p.Arg265=
NM_001122757.3:c.871C>A	NP_001116229.1:p.Arg291=