Canonical Allele Identifier: CA544801217
Gene: POU1F1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2908288
ClinVar RCV Id: RCV003729701
dbSNP Id: rs376889886
gnomAD v2: 3-87309259-C-CG
gnomAD v3: 3-87260109-C-CG
gnomAD v4: 3-87260109-C-CG
MyVariant Identifiers: chr3:g.87309260_87309261insG (hg19) chr3:g.87309259_87309260insG (hg19) chr3:g.87260110_87260111insG (hg38) chr3:g.87260109_87260110insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260115dup , CM000665.2:g.87260115dup GRCh38
NC_000003.11:g.87309265dup , CM000665.1:g.87309265dup GRCh37
NC_000003.10:g.87391955dup NCBI36
NG_008225.2:g.21478dup

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.744-6dup ENSP00000342931.3:n.744-6dup
ENST00000350375.7:c.666-6dup MANE Select ENSP00000263781.2:n.666-6dup
ENST00000344265.7:c.744-6dup ENSP00000342931.3:n.744-6dup
ENST00000350375.6:c.666-6dup ENSP00000263781.2:n.666-6dup
ENST00000560656.1:c.440-6dup ENSP00000452610.1:n.440-6dup
ENST00000561167.5:c.441-6dup ENSP00000454072.1:n.441-6dup
NM_000306.3:c.666-6dup NP_000297.1:n.666-6dup
NM_001122757.2:c.744-6dup NP_001116229.1:n.744-6dup
NM_000306.4:c.666-6dup MANE Select NP_000297.1:n.666-6dup
NM_001122757.3:c.744-6dup NP_001116229.1:n.744-6dup
Search 100 bp 5'
Search 100 bp 3'