Canonical Allele Identifier: CA353698171
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259997A>G , CM000665.2:g.87259997A>G GRCh38
NC_000003.11:g.87309147A>G , CM000665.1:g.87309147A>G GRCh37
NC_000003.10:g.87391837A>G NCBI36
NG_008225.2:g.21591T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.851T>C ENSP00000342931.3:p.Val284Ala
ENST00000350375.7:c.773T>C MANE Select ENSP00000263781.2:p.Val258Ala
ENST00000344265.7:c.851T>C ENSP00000342931.3:p.Val284Ala
ENST00000350375.6:c.773T>C ENSP00000263781.2:p.Val258Ala
ENST00000560656.1:c.547T>C ENSP00000452610.1:n.547T>C
ENST00000561167.5:c.548T>C ENSP00000454072.1:p.Val183Ala
NM_000306.3:c.773T>C NP_000297.1:p.Val258Ala
NM_001122757.2:c.851T>C NP_001116229.1:p.Val284Ala
NM_000306.4:c.773T>C MANE Select NP_000297.1:p.Val258Ala
NM_001122757.3:c.851T>C NP_001116229.1:p.Val284Ala