Canonical Allele Identifier: CA353698123

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309126C>G (hg19) ; chr3:g.87259976C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259976C>G , CM000665.2:g.87259976C>G	GRCh38
NC_000003.11:g.87309126C>G , CM000665.1:g.87309126C>G	GRCh37
NC_000003.10:g.87391816C>G	NCBI36
NG_008225.2:g.21612G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.872G>C	ENSP00000342931.3:p.Arg291Pro
ENST00000350375.7:c.794G>C MANE Select	ENSP00000263781.2:p.Arg265Pro
ENST00000344265.7:c.872G>C	ENSP00000342931.3:p.Arg291Pro
ENST00000350375.6:c.794G>C	ENSP00000263781.2:p.Arg265Pro
ENST00000560656.1:c.568G>C	ENSP00000452610.1:n.568G>C
ENST00000561167.5:c.569G>C	ENSP00000454072.1:p.Arg190Pro
NM_000306.3:c.794G>C	NP_000297.1:p.Arg265Pro
NM_001122757.2:c.872G>C	NP_001116229.1:p.Arg291Pro
NM_000306.4:c.794G>C MANE Select	NP_000297.1:p.Arg265Pro
NM_001122757.3:c.872G>C	NP_001116229.1:p.Arg291Pro