Canonical Allele Identifier: CA434575732

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87311336A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262186A>T , CM000665.2:g.87262186A>T	GRCh38
NC_000003.11:g.87311336A>T , CM000665.1:g.87311336A>T	GRCh37
NC_000003.10:g.87394026A>T	NCBI36
NG_008225.2:g.19402T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.567T>A	ENSP00000342931.3:p.Ser189=
ENST00000350375.7:c.489T>A MANE Select	ENSP00000263781.2:p.Ser163=
ENST00000344265.7:c.567T>A	ENSP00000342931.3:p.Ser189=
ENST00000350375.6:c.489T>A	ENSP00000263781.2:p.Ser163=
ENST00000560656.1:c.440-2082T>A	ENSP00000452610.1:n.440-2082T>A
ENST00000561167.5:c.264T>A	ENSP00000454072.1:p.Ser88=
NM_000306.3:c.489T>A	NP_000297.1:p.Ser163=
NM_001122757.2:c.567T>A	NP_001116229.1:p.Ser189=
NM_000306.4:c.489T>A MANE Select	NP_000297.1:p.Ser163=
NM_001122757.3:c.567T>A	NP_001116229.1:p.Ser189=