Canonical Allele Identifier: CA353692740
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1559614663

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262092C>G , CM000665.2:g.87262092C>G GRCh38
NC_000003.11:g.87311242C>G , CM000665.1:g.87311242C>G GRCh37
NC_000003.10:g.87393932C>G NCBI36
NG_008225.2:g.19496G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.661G>C ENSP00000342931.3:p.Glu221Gln
ENST00000350375.7:c.583G>C MANE Select ENSP00000263781.2:p.Glu195Gln
ENST00000344265.7:c.661G>C ENSP00000342931.3:p.Glu221Gln
ENST00000350375.6:c.583G>C ENSP00000263781.2:p.Glu195Gln
ENST00000560656.1:c.440-1988G>C ENSP00000452610.1:n.440-1988G>C
ENST00000561167.5:c.358G>C ENSP00000454072.1:p.Glu120Gln
NM_000306.3:c.583G>C NP_000297.1:p.Glu195Gln
NM_001122757.2:c.661G>C NP_001116229.1:p.Glu221Gln
NM_000306.4:c.583G>C MANE Select NP_000297.1:p.Glu195Gln
NM_001122757.3:c.661G>C NP_001116229.1:p.Glu221Gln