Canonical Allele Identifier: CA353693563

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87313462A>T (hg19) ; chr3:g.87264312A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87264312A>T , CM000665.2:g.87264312A>T	GRCh38
NC_000003.11:g.87313462A>T , CM000665.1:g.87313462A>T	GRCh37
NC_000003.10:g.87396152A>T	NCBI36
NG_008225.2:g.17276T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.493T>A	ENSP00000342931.3:p.Phe165Ile
ENST00000350375.7:c.415T>A MANE Select	ENSP00000263781.2:p.Phe139Ile
ENST00000344265.7:c.493T>A	ENSP00000342931.3:p.Phe165Ile
ENST00000350375.6:c.415T>A	ENSP00000263781.2:p.Phe139Ile
ENST00000560656.1:c.415T>A	ENSP00000452610.1:p.Phe139Ile
ENST00000561167.5:c.215-2077T>A	ENSP00000454072.1:n.215-2077T>A
NM_000306.3:c.415T>A	NP_000297.1:p.Phe139Ile
NM_001122757.2:c.493T>A	NP_001116229.1:p.Phe165Ile
NM_000306.4:c.415T>A MANE Select	NP_000297.1:p.Phe139Ile
NM_001122757.3:c.493T>A	NP_001116229.1:p.Phe165Ile