Canonical Allele Identifier: CA434579455
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259981-G-A
MyVariant Identifiers: chr3:g.87309131G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259981G>A , CM000665.2:g.87259981G>A GRCh38
NC_000003.11:g.87309131G>A , CM000665.1:g.87309131G>A GRCh37
NC_000003.10:g.87391821G>A NCBI36
NG_008225.2:g.21607C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.867C>T ENSP00000342931.3:p.Cys289=
ENST00000350375.7:c.789C>T MANE Select ENSP00000263781.2:p.Cys263=
ENST00000344265.7:c.867C>T ENSP00000342931.3:p.Cys289=
ENST00000350375.6:c.789C>T ENSP00000263781.2:p.Cys263=
ENST00000560656.1:c.563C>T ENSP00000452610.1:n.563C>T
ENST00000561167.5:c.564C>T ENSP00000454072.1:p.Cys188=
NM_000306.3:c.789C>T NP_000297.1:p.Cys263=
NM_001122757.2:c.867C>T NP_001116229.1:p.Cys289=
NM_000306.4:c.789C>T MANE Select NP_000297.1:p.Cys263=
NM_001122757.3:c.867C>T NP_001116229.1:p.Cys289=