Canonical Allele Identifier: CA353698290
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260046G>C , CM000665.2:g.87260046G>C GRCh38
NC_000003.11:g.87309196G>C , CM000665.1:g.87309196G>C GRCh37
NC_000003.10:g.87391886G>C NCBI36
NG_008225.2:g.21542C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.802C>G ENSP00000342931.3:p.Gln268Glu
ENST00000350375.7:c.724C>G MANE Select ENSP00000263781.2:p.Gln242Glu
ENST00000344265.7:c.802C>G ENSP00000342931.3:p.Gln268Glu
ENST00000350375.6:c.724C>G ENSP00000263781.2:p.Gln242Glu
ENST00000560656.1:c.498C>G ENSP00000452610.1:p.Leu166=
ENST00000561167.5:c.499C>G ENSP00000454072.1:p.Gln167Glu
NM_000306.3:c.724C>G NP_000297.1:p.Gln242Glu
NM_001122757.2:c.802C>G NP_001116229.1:p.Gln268Glu
NM_000306.4:c.724C>G MANE Select NP_000297.1:p.Gln242Glu
NM_001122757.3:c.802C>G NP_001116229.1:p.Gln268Glu