Canonical Allele Identifier: CA2554586318
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261964_87261965insA , CM000665.2:g.87261964_87261965insA GRCh38
NC_000003.11:g.87311114_87311115insA , CM000665.1:g.87311114_87311115insA GRCh37
NC_000003.10:g.87393804_87393805insA NCBI36
NG_008225.2:g.19623_19624insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+106_682+107insT ENSP00000342931.3:n.682+106_682+107insT
ENST00000350375.7:c.604+106_604+107insT MANE Select ENSP00000263781.2:n.604+106_604+107insT
ENST00000344265.7:c.682+106_682+107insT ENSP00000342931.3:n.682+106_682+107insT
ENST00000350375.6:c.604+106_604+107insT ENSP00000263781.2:n.604+106_604+107insT
ENST00000560656.1:c.440-1861_440-1860insT ENSP00000452610.1:n.440-1861_440-1860insT
ENST00000561167.5:c.379+106_379+107insT ENSP00000454072.1:n.379+106_379+107insT
NM_000306.3:c.604+106_604+107insT NP_000297.1:n.604+106_604+107insT
NM_001122757.2:c.682+106_682+107insT NP_001116229.1:n.682+106_682+107insT
NM_000306.4:c.604+106_604+107insT MANE Select NP_000297.1:n.604+106_604+107insT
NM_001122757.3:c.682+106_682+107insT NP_001116229.1:n.682+106_682+107insT