Canonical Allele Identifier: CA353698226
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260022C>T , CM000665.2:g.87260022C>T GRCh38
NC_000003.11:g.87309172C>T , CM000665.1:g.87309172C>T GRCh37
NC_000003.10:g.87391862C>T NCBI36
NG_008225.2:g.21566G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.826G>A ENSP00000342931.3:p.Glu276Lys
ENST00000350375.7:c.748G>A MANE Select ENSP00000263781.2:p.Glu250Lys
ENST00000344265.7:c.826G>A ENSP00000342931.3:p.Glu276Lys
ENST00000350375.6:c.748G>A ENSP00000263781.2:p.Glu250Lys
ENST00000560656.1:c.522G>A ENSP00000452610.1:n.522G>A
ENST00000561167.5:c.523G>A ENSP00000454072.1:p.Glu175Lys
NM_000306.3:c.748G>A NP_000297.1:p.Glu250Lys
NM_001122757.2:c.826G>A NP_001116229.1:p.Glu276Lys
NM_000306.4:c.748G>A MANE Select NP_000297.1:p.Glu250Lys
NM_001122757.3:c.826G>A NP_001116229.1:p.Glu276Lys