Canonical Allele Identifier: CA1381532911
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1706524069

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262076dup , CM000665.2:g.87262076dup GRCh38
NC_000003.11:g.87311226dup , CM000665.1:g.87311226dup GRCh37
NC_000003.10:g.87393916dup NCBI36
NG_008225.2:g.19512dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.677dup ENSP00000342931.3:p.Gly227ArgfsTer6
ENST00000350375.7:c.599dup MANE Select ENSP00000263781.2:p.Gly201ArgfsTer6
ENST00000344265.7:c.677dup ENSP00000342931.3:p.Gly227ArgfsTer6
ENST00000350375.6:c.599dup ENSP00000263781.2:p.Gly201ArgfsTer6
ENST00000560656.1:c.440-1972dup ENSP00000452610.1:n.440-1972dup
ENST00000561167.5:c.374dup ENSP00000454072.1:p.Gly126ArgfsTer6
NM_000306.3:c.599dup NP_000297.1:p.Gly201ArgfsTer6
NM_001122757.2:c.677dup NP_001116229.1:p.Gly227ArgfsTer6
NM_000306.4:c.599dup MANE Select NP_000297.1:p.Gly201ArgfsTer6
NM_001122757.3:c.677dup NP_001116229.1:p.Gly227ArgfsTer6