Canonical Allele Identifier: CA353698114
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259971G>C , CM000665.2:g.87259971G>C GRCh38
NC_000003.11:g.87309121G>C , CM000665.1:g.87309121G>C GRCh37
NC_000003.10:g.87391811G>C NCBI36
NG_008225.2:g.21617C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.877C>G ENSP00000342931.3:p.Gln293Glu
ENST00000350375.7:c.799C>G MANE Select ENSP00000263781.2:p.Gln267Glu
ENST00000344265.7:c.877C>G ENSP00000342931.3:p.Gln293Glu
ENST00000350375.6:c.799C>G ENSP00000263781.2:p.Gln267Glu
ENST00000560656.1:c.573C>G ENSP00000452610.1:n.573C>G
ENST00000561167.5:c.574C>G ENSP00000454072.1:p.Gln192Glu
NM_000306.3:c.799C>G NP_000297.1:p.Gln267Glu
NM_001122757.2:c.877C>G NP_001116229.1:p.Gln293Glu
NM_000306.4:c.799C>G MANE Select NP_000297.1:p.Gln267Glu
NM_001122757.3:c.877C>G NP_001116229.1:p.Gln293Glu