Canonical Allele Identifier: CA2666629892
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87264263-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264263C>T , CM000665.2:g.87264263C>T GRCh38
NC_000003.11:g.87313413C>T , CM000665.1:g.87313413C>T GRCh37
NC_000003.10:g.87396103C>T NCBI36
NG_008225.2:g.17325G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.517+25G>A ENSP00000342931.3:n.517+25G>A
ENST00000350375.7:c.439+25G>A MANE Select ENSP00000263781.2:n.439+25G>A
ENST00000344265.7:c.517+25G>A ENSP00000342931.3:n.517+25G>A
ENST00000350375.6:c.439+25G>A ENSP00000263781.2:n.439+25G>A
ENST00000560656.1:c.439+25G>A ENSP00000452610.1:n.439+25G>A
ENST00000561167.5:c.215-2028G>A ENSP00000454072.1:n.215-2028G>A
NM_000306.3:c.439+25G>A NP_000297.1:n.439+25G>A
NM_001122757.2:c.517+25G>A NP_001116229.1:n.517+25G>A
NM_000306.4:c.439+25G>A MANE Select NP_000297.1:n.439+25G>A
NM_001122757.3:c.517+25G>A NP_001116229.1:n.517+25G>A
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