Canonical Allele Identifier: CA2666629257
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259699-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259701del , CM000665.2:g.87259701del GRCh38
NC_000003.11:g.87308851del , CM000665.1:g.87308851del GRCh37
NC_000003.10:g.87391541del NCBI36
NG_008225.2:g.21888del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*194del ENSP00000342931.3:n.*194del
ENST00000350375.7:c.*194del MANE Select ENSP00000263781.2:n.*194del
ENST00000350375.6:c.*194del ENSP00000263781.2:n.*194del
NM_000306.3:c.*194del NP_000297.1:n.*194del
NM_001122757.2:c.*194del NP_001116229.1:n.*194del
NM_000306.4:c.*194del MANE Select NP_000297.1:n.*194del
NM_001122757.3:c.*194del NP_001116229.1:n.*194del
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