Canonical Allele Identifier: CA353692747

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87311246C>G (hg19) ; chr3:g.87262096C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262096C>G , CM000665.2:g.87262096C>G	GRCh38
NC_000003.11:g.87311246C>G , CM000665.1:g.87311246C>G	GRCh37
NC_000003.10:g.87393936C>G	NCBI36
NG_008225.2:g.19492G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.657G>C	ENSP00000342931.3:p.Trp219Cys
ENST00000350375.7:c.579G>C MANE Select	ENSP00000263781.2:p.Trp193Cys
ENST00000344265.7:c.657G>C	ENSP00000342931.3:p.Trp219Cys
ENST00000350375.6:c.579G>C	ENSP00000263781.2:p.Trp193Cys
ENST00000560656.1:c.440-1992G>C	ENSP00000452610.1:n.440-1992G>C
ENST00000561167.5:c.354G>C	ENSP00000454072.1:p.Trp118Cys
NM_000306.3:c.579G>C	NP_000297.1:p.Trp193Cys
NM_001122757.2:c.657G>C	NP_001116229.1:p.Trp219Cys
NM_000306.4:c.579G>C MANE Select	NP_000297.1:p.Trp193Cys
NM_001122757.3:c.657G>C	NP_001116229.1:p.Trp219Cys