Canonical Allele Identifier: CA2666629859

Gene: POU1F1

Linked Data

• gnomAD v4: 3-87264202-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87264202_87264203insT , CM000665.2:g.87264202_87264203insT	GRCh38
NC_000003.11:g.87313352_87313353insT , CM000665.1:g.87313352_87313353insT	GRCh37
NC_000003.10:g.87396042_87396043insT	NCBI36
NG_008225.2:g.17385_17386insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.517+85_517+86insA	ENSP00000342931.3:n.517+85_517+86insA
ENST00000350375.7:c.439+85_439+86insA MANE Select	ENSP00000263781.2:n.439+85_439+86insA
ENST00000344265.7:c.517+85_517+86insA	ENSP00000342931.3:n.517+85_517+86insA
ENST00000350375.6:c.439+85_439+86insA	ENSP00000263781.2:n.439+85_439+86insA
ENST00000560656.1:c.439+85_439+86insA	ENSP00000452610.1:n.439+85_439+86insA
ENST00000561167.5:c.215-1968_215-1967insA	ENSP00000454072.1:n.215-1968_215-1967insA
NM_000306.3:c.439+85_439+86insA	NP_000297.1:n.439+85_439+86insA
NM_001122757.2:c.517+85_517+86insA	NP_001116229.1:n.517+85_517+86insA
NM_000306.4:c.439+85_439+86insA MANE Select	NP_000297.1:n.439+85_439+86insA
NM_001122757.3:c.517+85_517+86insA	NP_001116229.1:n.517+85_517+86insA