Canonical Allele Identifier: CA2666629692
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261972_87261974dup , CM000665.2:g.87261972_87261974dup GRCh38
NC_000003.11:g.87311122_87311124dup , CM000665.1:g.87311122_87311124dup GRCh37
NC_000003.10:g.87393812_87393814dup NCBI36
NG_008225.2:g.19618_19620dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+101_682+103dup ENSP00000342931.3:n.682+101_682+103dup
ENST00000350375.7:c.604+101_604+103dup MANE Select ENSP00000263781.2:n.604+101_604+103dup
ENST00000344265.7:c.682+101_682+103dup ENSP00000342931.3:n.682+101_682+103dup
ENST00000350375.6:c.604+101_604+103dup ENSP00000263781.2:n.604+101_604+103dup
ENST00000560656.1:c.440-1866_440-1864dup ENSP00000452610.1:n.440-1866_440-1864dup
ENST00000561167.5:c.379+101_379+103dup ENSP00000454072.1:n.379+101_379+103dup
NM_000306.3:c.604+101_604+103dup NP_000297.1:n.604+101_604+103dup
NM_001122757.2:c.682+101_682+103dup NP_001116229.1:n.682+101_682+103dup
NM_000306.4:c.604+101_604+103dup MANE Select NP_000297.1:n.604+101_604+103dup
NM_001122757.3:c.682+101_682+103dup NP_001116229.1:n.682+101_682+103dup