Canonical Allele Identifier: CA911577596

Gene: POU1F1

Linked Data

• dbSNP Id: rs1196677695
• gnomAD v3: 3-87261900-C-CT
• gnomAD v4: 3-87261900-C-CT
• MyVariant Identifiers: chr3:g.87311050_87311051insT (hg19) ; chr3:g.87261900_87261901insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87261906dup , CM000665.2:g.87261906dup	GRCh38
NC_000003.11:g.87311056dup , CM000665.1:g.87311056dup	GRCh37
NC_000003.10:g.87393746dup	NCBI36
NG_008225.2:g.19687dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000344265.8:c.682+170dup	ENSP00000342931.3:n.682+170dup
ENST00000350375.7:c.604+170dup MANE Select	ENSP00000263781.2:n.604+170dup
ENST00000344265.7:c.682+170dup	ENSP00000342931.3:n.682+170dup
ENST00000350375.6:c.604+170dup	ENSP00000263781.2:n.604+170dup
ENST00000560656.1:c.440-1797dup	ENSP00000452610.1:n.440-1797dup
ENST00000561167.5:c.379+170dup	ENSP00000454072.1:n.379+170dup
NM_000306.3:c.604+170dup	NP_000297.1:n.604+170dup
NM_001122757.2:c.682+170dup	NP_001116229.1:n.682+170dup
NM_000306.4:c.604+170dup MANE Select	NP_000297.1:n.604+170dup
NM_001122757.3:c.682+170dup	NP_001116229.1:n.682+170dup