Canonical Allele Identifier: CA911575009
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1313701778
gnomAD v4: 3-87259735-ATTG-A
MyVariant Identifiers: chr3:g.87308886_87308888del (hg19) chr3:g.87259736_87259738del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259739_87259741del , CM000665.2:g.87259739_87259741del GRCh38
NC_000003.11:g.87308889_87308891del , CM000665.1:g.87308889_87308891del GRCh37
NC_000003.10:g.87391579_87391581del NCBI36
NG_008225.2:g.21850_21852del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*156_*158del ENSP00000342931.3:n.*156_*158del
ENST00000350375.7:c.*156_*158del MANE Select ENSP00000263781.2:n.*156_*158del
ENST00000350375.6:c.*156_*158del ENSP00000263781.2:n.*156_*158del
NM_000306.3:c.*156_*158del NP_000297.1:n.*156_*158del
NM_001122757.2:c.*156_*158del NP_001116229.1:n.*156_*158del
NM_000306.4:c.*156_*158del MANE Select NP_000297.1:n.*156_*158del
NM_001122757.3:c.*156_*158del NP_001116229.1:n.*156_*158del
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