Canonical Allele Identifier: CA434627012
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87264325-C-T
MyVariant Identifiers: chr3:g.87313475C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264325C>T , CM000665.2:g.87264325C>T GRCh38
NC_000003.11:g.87313475C>T , CM000665.1:g.87313475C>T GRCh37
NC_000003.10:g.87396165C>T NCBI36
NG_008225.2:g.17263G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.480G>A ENSP00000342931.3:p.Lys160=
ENST00000350375.7:c.402G>A MANE Select ENSP00000263781.2:p.Lys134=
ENST00000344265.7:c.480G>A ENSP00000342931.3:p.Lys160=
ENST00000350375.6:c.402G>A ENSP00000263781.2:p.Lys134=
ENST00000560656.1:c.402G>A ENSP00000452610.1:p.Lys134=
ENST00000561167.5:c.215-2090G>A ENSP00000454072.1:n.215-2090G>A
NM_000306.3:c.402G>A NP_000297.1:p.Lys134=
NM_001122757.2:c.480G>A NP_001116229.1:p.Lys160=
NM_000306.4:c.402G>A MANE Select NP_000297.1:p.Lys134=
NM_001122757.3:c.480G>A NP_001116229.1:p.Lys160=