Canonical Allele Identifier: CA911575035
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1303026068
gnomAD v4: 3-87259750-TTTTTAAAAAAAAGTGGAAAA-T
MyVariant Identifiers: chr3:g.87308901_87308920del (hg19) chr3:g.87259751_87259770del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259751_87259770del , CM000665.2:g.87259751_87259770del GRCh38
NC_000003.11:g.87308901_87308920del , CM000665.1:g.87308901_87308920del GRCh37
NC_000003.10:g.87391591_87391610del NCBI36
NG_008225.2:g.21818_21837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*124_*143del ENSP00000342931.3:n.*124_*143del
ENST00000350375.7:c.*124_*143del MANE Select ENSP00000263781.2:n.*124_*143del
ENST00000344265.7:c.*124_*143del ENSP00000342931.3:n.*124_*143del
ENST00000350375.6:c.*124_*143del ENSP00000263781.2:n.*124_*143del
NM_000306.3:c.*124_*143del NP_000297.1:n.*124_*143del
NM_001122757.2:c.*124_*143del NP_001116229.1:n.*124_*143del
NM_000306.4:c.*124_*143del MANE Select NP_000297.1:n.*124_*143del
NM_001122757.3:c.*124_*143del NP_001116229.1:n.*124_*143del
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