Canonical Allele Identifier: CA353698256

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309184T>G (hg19) ; chr3:g.87260034T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87260034T>G , CM000665.2:g.87260034T>G	GRCh38
NC_000003.11:g.87309184T>G , CM000665.1:g.87309184T>G	GRCh37
NC_000003.10:g.87391874T>G	NCBI36
NG_008225.2:g.21554A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.814A>C	ENSP00000342931.3:p.Arg272=
ENST00000350375.7:c.736A>C MANE Select	ENSP00000263781.2:p.Arg246=
ENST00000344265.7:c.814A>C	ENSP00000342931.3:p.Arg272=
ENST00000350375.6:c.736A>C	ENSP00000263781.2:p.Arg246=
ENST00000560656.1:c.510A>C	ENSP00000452610.1:p.Ter170Cys
ENST00000561167.5:c.511A>C	ENSP00000454072.1:p.Arg171=
NM_000306.3:c.736A>C	NP_000297.1:p.Arg246=
NM_001122757.2:c.814A>C	NP_001116229.1:p.Arg272=
NM_000306.4:c.736A>C MANE Select	NP_000297.1:p.Arg246=
NM_001122757.3:c.814A>C	NP_001116229.1:p.Arg272=