Canonical Allele Identifier: CA79036656
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs772595095
MyVariant Identifiers: chr3:g.87311079del (hg19) chr3:g.87261929del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261930del , CM000665.2:g.87261930del GRCh38
NC_000003.11:g.87311080del , CM000665.1:g.87311080del GRCh37
NC_000003.10:g.87393770del NCBI36
NG_008225.2:g.19659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+142del ENSP00000342931.3:n.682+142del
ENST00000350375.7:c.604+142del MANE Select ENSP00000263781.2:n.604+142del
ENST00000344265.7:c.682+142del ENSP00000342931.3:n.682+142del
ENST00000350375.6:c.604+142del ENSP00000263781.2:n.604+142del
ENST00000560656.1:c.440-1825del ENSP00000452610.1:n.440-1825del
ENST00000561167.5:c.379+142del ENSP00000454072.1:n.379+142del
NM_000306.3:c.604+142del NP_000297.1:n.604+142del
NM_001122757.2:c.682+142del NP_001116229.1:n.682+142del
NM_000306.4:c.604+142del MANE Select NP_000297.1:n.604+142del
NM_001122757.3:c.682+142del NP_001116229.1:n.682+142del
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