Canonical Allele Identifier: CA353693092
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262215C>A , CM000665.2:g.87262215C>A GRCh38
NC_000003.11:g.87311365C>A , CM000665.1:g.87311365C>A GRCh37
NC_000003.10:g.87394055C>A NCBI36
NG_008225.2:g.19373G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.538G>T ENSP00000342931.3:p.Gly180Trp
ENST00000350375.7:c.460G>T MANE Select ENSP00000263781.2:p.Gly154Trp
ENST00000344265.7:c.538G>T ENSP00000342931.3:p.Gly180Trp
ENST00000350375.6:c.460G>T ENSP00000263781.2:p.Gly154Trp
ENST00000560656.1:c.439+2073G>T ENSP00000452610.1:n.439+2073G>T
ENST00000561167.5:c.235G>T ENSP00000454072.1:p.Gly79Trp
NM_000306.3:c.460G>T NP_000297.1:p.Gly154Trp
NM_001122757.2:c.538G>T NP_001116229.1:p.Gly180Trp
NM_000306.4:c.460G>T MANE Select NP_000297.1:p.Gly154Trp
NM_001122757.3:c.538G>T NP_001116229.1:p.Gly180Trp