Canonical Allele Identifier: CA911575023
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1309375356
gnomAD v3: 3-87259742-GTTTCT-G
gnomAD v4: 3-87259742-GTTTCT-G
MyVariant Identifiers: chr3:g.87308893_87308897del (hg19) chr3:g.87259743_87259747del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259746_87259750del , CM000665.2:g.87259746_87259750del GRCh38
NC_000003.11:g.87308896_87308900del , CM000665.1:g.87308896_87308900del GRCh37
NC_000003.10:g.87391586_87391590del NCBI36
NG_008225.2:g.21841_21845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*147_*151del ENSP00000342931.3:n.*147_*151del
ENST00000350375.7:c.*147_*151del MANE Select ENSP00000263781.2:n.*147_*151del
ENST00000344265.7:c.*147_*151del ENSP00000342931.3:n.*147_*151del
ENST00000350375.6:c.*147_*151del ENSP00000263781.2:n.*147_*151del
NM_000306.3:c.*147_*151del NP_000297.1:n.*147_*151del
NM_001122757.2:c.*147_*151del NP_001116229.1:n.*147_*151del
NM_000306.4:c.*147_*151del MANE Select NP_000297.1:n.*147_*151del
NM_001122757.3:c.*147_*151del NP_001116229.1:n.*147_*151del
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