Canonical Allele Identifier: CA353698002

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309073T>C (hg19) ; chr3:g.87259923T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259923T>C , CM000665.2:g.87259923T>C	GRCh38
NC_000003.11:g.87309073T>C , CM000665.1:g.87309073T>C	GRCh37
NC_000003.10:g.87391763T>C	NCBI36
NG_008225.2:g.21665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.925A>G	ENSP00000342931.3:p.Ile309Val
ENST00000350375.7:c.847A>G MANE Select	ENSP00000263781.2:p.Ile283Val
ENST00000344265.7:c.925A>G	ENSP00000342931.3:p.Ile309Val
ENST00000350375.6:c.847A>G	ENSP00000263781.2:p.Ile283Val
ENST00000560656.1:c.621A>G	ENSP00000452610.1:n.621A>G
ENST00000561167.5:c.622A>G	ENSP00000454072.1:p.Ile208Val
NM_000306.3:c.847A>G	NP_000297.1:p.Ile283Val
NM_001122757.2:c.925A>G	NP_001116229.1:p.Ile309Val
NM_000306.4:c.847A>G MANE Select	NP_000297.1:p.Ile283Val
NM_001122757.3:c.925A>G	NP_001116229.1:p.Ile309Val