Canonical Allele Identifier: CA353698155

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309138C>G (hg19) ; chr3:g.87259988C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259988C>G , CM000665.2:g.87259988C>G	GRCh38
NC_000003.11:g.87309138C>G , CM000665.1:g.87309138C>G	GRCh37
NC_000003.10:g.87391828C>G	NCBI36
NG_008225.2:g.21600G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.860G>C	ENSP00000342931.3:p.Trp287Ser
ENST00000350375.7:c.782G>C MANE Select	ENSP00000263781.2:p.Trp261Ser
ENST00000344265.7:c.860G>C	ENSP00000342931.3:p.Trp287Ser
ENST00000350375.6:c.782G>C	ENSP00000263781.2:p.Trp261Ser
ENST00000560656.1:c.556G>C	ENSP00000452610.1:n.556G>C
ENST00000561167.5:c.557G>C	ENSP00000454072.1:p.Trp186Ser
NM_000306.3:c.782G>C	NP_000297.1:p.Trp261Ser
NM_001122757.2:c.860G>C	NP_001116229.1:p.Trp287Ser
NM_000306.4:c.782G>C MANE Select	NP_000297.1:p.Trp261Ser
NM_001122757.3:c.860G>C	NP_001116229.1:p.Trp287Ser