Canonical Allele Identifier: CA353698220
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.828A>T ENSP00000342931.3:p.Glu276Asp
ENST00000350375.7:c.750A>T MANE Select ENSP00000263781.2:p.Glu250Asp
ENST00000344265.7:c.828A>T ENSP00000342931.3:p.Glu276Asp
ENST00000350375.6:c.750A>T ENSP00000263781.2:p.Glu250Asp
ENST00000560656.1:c.524A>T ENSP00000452610.1:n.524A>T
ENST00000561167.5:c.525A>T ENSP00000454072.1:p.Glu175Asp
NM_000306.3:c.750A>T NP_000297.1:p.Glu250Asp
NM_001122757.2:c.828A>T NP_001116229.1:p.Glu276Asp
NM_000306.4:c.750A>T MANE Select NP_000297.1:p.Glu250Asp
NM_001122757.3:c.828A>T NP_001116229.1:p.Glu276Asp