Canonical Allele Identifier: CA353698138

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309132C>T (hg19) ; chr3:g.87259982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259982C>T , CM000665.2:g.87259982C>T	GRCh38
NC_000003.11:g.87309132C>T , CM000665.1:g.87309132C>T	GRCh37
NC_000003.10:g.87391822C>T	NCBI36
NG_008225.2:g.21606G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.866G>A	ENSP00000342931.3:p.Cys289Tyr
ENST00000350375.7:c.788G>A MANE Select	ENSP00000263781.2:p.Cys263Tyr
ENST00000344265.7:c.866G>A	ENSP00000342931.3:p.Cys289Tyr
ENST00000350375.6:c.788G>A	ENSP00000263781.2:p.Cys263Tyr
ENST00000560656.1:c.562G>A	ENSP00000452610.1:n.562G>A
ENST00000561167.5:c.563G>A	ENSP00000454072.1:p.Cys188Tyr
NM_000306.3:c.788G>A	NP_000297.1:p.Cys263Tyr
NM_001122757.2:c.866G>A	NP_001116229.1:p.Cys289Tyr
NM_000306.4:c.788G>A MANE Select	NP_000297.1:p.Cys263Tyr
NM_001122757.3:c.866G>A	NP_001116229.1:p.Cys289Tyr