Canonical Allele Identifier: CA353698286
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260045T>A , CM000665.2:g.87260045T>A GRCh38
NC_000003.11:g.87309195T>A , CM000665.1:g.87309195T>A GRCh37
NC_000003.10:g.87391885T>A NCBI36
NG_008225.2:g.21543A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.803A>T ENSP00000342931.3:p.Gln268Leu
ENST00000350375.7:c.725A>T MANE Select ENSP00000263781.2:p.Gln242Leu
ENST00000344265.7:c.803A>T ENSP00000342931.3:p.Gln268Leu
ENST00000350375.6:c.725A>T ENSP00000263781.2:p.Gln242Leu
ENST00000560656.1:c.499A>T ENSP00000452610.1:p.Lys167Ter
ENST00000561167.5:c.500A>T ENSP00000454072.1:p.Gln167Leu
NM_000306.3:c.725A>T NP_000297.1:p.Gln242Leu
NM_001122757.2:c.803A>T NP_001116229.1:p.Gln268Leu
NM_000306.4:c.725A>T MANE Select NP_000297.1:p.Gln242Leu
NM_001122757.3:c.803A>T NP_001116229.1:p.Gln268Leu