Canonical Allele Identifier: CA434579638

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309170T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87260020T>C , CM000665.2:g.87260020T>C	GRCh38
NC_000003.11:g.87309170T>C , CM000665.1:g.87309170T>C	GRCh37
NC_000003.10:g.87391860T>C	NCBI36
NG_008225.2:g.21568A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.828A>G	ENSP00000342931.3:p.Glu276=
ENST00000350375.7:c.750A>G MANE Select	ENSP00000263781.2:p.Glu250=
ENST00000344265.7:c.828A>G	ENSP00000342931.3:p.Glu276=
ENST00000350375.6:c.750A>G	ENSP00000263781.2:p.Glu250=
ENST00000560656.1:c.524A>G	ENSP00000452610.1:n.524A>G
ENST00000561167.5:c.525A>G	ENSP00000454072.1:p.Glu175=
NM_000306.3:c.750A>G	NP_000297.1:p.Glu250=
NM_001122757.2:c.828A>G	NP_001116229.1:p.Glu276=
NM_000306.4:c.750A>G MANE Select	NP_000297.1:p.Glu250=
NM_001122757.3:c.828A>G	NP_001116229.1:p.Glu276=