Canonical Allele Identifier: CA2666629335
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259772-TA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259775del , CM000665.2:g.87259775del GRCh38
NC_000003.11:g.87308925del , CM000665.1:g.87308925del GRCh37
NC_000003.10:g.87391615del NCBI36
NG_008225.2:g.21815del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*121del ENSP00000342931.3:n.*121del
ENST00000350375.7:c.*121del MANE Select ENSP00000263781.2:n.*121del
ENST00000344265.7:c.*121del ENSP00000342931.3:n.*121del
ENST00000350375.6:c.*121del ENSP00000263781.2:n.*121del
NM_000306.3:c.*121del NP_000297.1:n.*121del
NM_001122757.2:c.*121del NP_001116229.1:n.*121del
NM_000306.4:c.*121del MANE Select NP_000297.1:n.*121del
NM_001122757.3:c.*121del NP_001116229.1:n.*121del
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