Canonical Allele Identifier: CA353698184
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260003T>C , CM000665.2:g.87260003T>C GRCh38
NC_000003.11:g.87309153T>C , CM000665.1:g.87309153T>C GRCh37
NC_000003.10:g.87391843T>C NCBI36
NG_008225.2:g.21585A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.845A>G ENSP00000342931.3:p.Glu282Gly
ENST00000350375.7:c.767A>G MANE Select ENSP00000263781.2:p.Glu256Gly
ENST00000344265.7:c.845A>G ENSP00000342931.3:p.Glu282Gly
ENST00000350375.6:c.767A>G ENSP00000263781.2:p.Glu256Gly
ENST00000560656.1:c.541A>G ENSP00000452610.1:n.541A>G
ENST00000561167.5:c.542A>G ENSP00000454072.1:p.Glu181Gly
NM_000306.3:c.767A>G NP_000297.1:p.Glu256Gly
NM_001122757.2:c.845A>G NP_001116229.1:p.Glu282Gly
NM_000306.4:c.767A>G MANE Select NP_000297.1:p.Glu256Gly
NM_001122757.3:c.845A>G NP_001116229.1:p.Glu282Gly