Canonical Allele Identifier: CA1381566412
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1706522051

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261967dup , CM000665.2:g.87261967dup GRCh38
NC_000003.11:g.87311117dup , CM000665.1:g.87311117dup GRCh37
NC_000003.10:g.87393807dup NCBI36
NG_008225.2:g.19622dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+105dup ENSP00000342931.3:n.682+105dup
ENST00000350375.7:c.604+105dup MANE Select ENSP00000263781.2:n.604+105dup
ENST00000344265.7:c.682+105dup ENSP00000342931.3:n.682+105dup
ENST00000350375.6:c.604+105dup ENSP00000263781.2:n.604+105dup
ENST00000560656.1:c.440-1862dup ENSP00000452610.1:n.440-1862dup
ENST00000561167.5:c.379+105dup ENSP00000454072.1:n.379+105dup
NM_000306.3:c.604+105dup NP_000297.1:n.604+105dup
NM_001122757.2:c.682+105dup NP_001116229.1:n.682+105dup
NM_000306.4:c.604+105dup MANE Select NP_000297.1:n.604+105dup
NM_001122757.3:c.682+105dup NP_001116229.1:n.682+105dup