Canonical Allele Identifier: CA353693037

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87311349G>T (hg19) ; chr3:g.87262199G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262199G>T , CM000665.2:g.87262199G>T	GRCh38
NC_000003.11:g.87311349G>T , CM000665.1:g.87311349G>T	GRCh37
NC_000003.10:g.87394039G>T	NCBI36
NG_008225.2:g.19389C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.554C>A	ENSP00000342931.3:p.Ala185Asp
ENST00000350375.7:c.476C>A MANE Select	ENSP00000263781.2:p.Ala159Asp
ENST00000344265.7:c.554C>A	ENSP00000342931.3:p.Ala185Asp
ENST00000350375.6:c.476C>A	ENSP00000263781.2:p.Ala159Asp
ENST00000560656.1:c.439+2089C>A	ENSP00000452610.1:n.439+2089C>A
ENST00000561167.5:c.251C>A	ENSP00000454072.1:p.Ala84Asp
NM_000306.3:c.476C>A	NP_000297.1:p.Ala159Asp
NM_001122757.2:c.554C>A	NP_001116229.1:p.Ala185Asp
NM_000306.4:c.476C>A MANE Select	NP_000297.1:p.Ala159Asp
NM_001122757.3:c.554C>A	NP_001116229.1:p.Ala185Asp