Canonical Allele Identifier: CA353698298

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309199A>T (hg19) ; chr3:g.87260049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87260049A>T , CM000665.2:g.87260049A>T	GRCh38
NC_000003.11:g.87309199A>T , CM000665.1:g.87309199A>T	GRCh37
NC_000003.10:g.87391889A>T	NCBI36
NG_008225.2:g.21539T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.799T>A	ENSP00000342931.3:p.Ser267Thr
ENST00000350375.7:c.721T>A MANE Select	ENSP00000263781.2:p.Ser241Thr
ENST00000344265.7:c.799T>A	ENSP00000342931.3:p.Ser267Thr
ENST00000350375.6:c.721T>A	ENSP00000263781.2:p.Ser241Thr
ENST00000560656.1:c.495T>A	ENSP00000452610.1:p.Leu165=
ENST00000561167.5:c.496T>A	ENSP00000454072.1:p.Ser166Thr
NM_000306.3:c.721T>A	NP_000297.1:p.Ser241Thr
NM_001122757.2:c.799T>A	NP_001116229.1:p.Ser267Thr
NM_000306.4:c.721T>A MANE Select	NP_000297.1:p.Ser241Thr
NM_001122757.3:c.799T>A	NP_001116229.1:p.Ser267Thr