Canonical Allele Identifier: CA2666629396
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87260120-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260120C>A , CM000665.2:g.87260120C>A GRCh38
NC_000003.11:g.87309270C>A , CM000665.1:g.87309270C>A GRCh37
NC_000003.10:g.87391960C>A NCBI36
NG_008225.2:g.21468G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.744-16G>T ENSP00000342931.3:n.744-16G>T
ENST00000350375.7:c.666-16G>T MANE Select ENSP00000263781.2:n.666-16G>T
ENST00000344265.7:c.744-16G>T ENSP00000342931.3:n.744-16G>T
ENST00000350375.6:c.666-16G>T ENSP00000263781.2:n.666-16G>T
ENST00000560656.1:c.440-16G>T ENSP00000452610.1:n.440-16G>T
ENST00000561167.5:c.441-16G>T ENSP00000454072.1:n.441-16G>T
NM_000306.3:c.666-16G>T NP_000297.1:n.666-16G>T
NM_001122757.2:c.744-16G>T NP_001116229.1:n.744-16G>T
NM_000306.4:c.666-16G>T MANE Select NP_000297.1:n.666-16G>T
NM_001122757.3:c.744-16G>T NP_001116229.1:n.744-16G>T