Canonical Allele Identifier: CA911577685

Gene: POU1F1

Linked Data

• dbSNP Id: rs1412215233
• gnomAD v3: 3-87262042-GCACAGCCTTCAGAGA-G
• gnomAD v4: 3-87262042-GCACAGCCTTCAGAGA-G
• MyVariant Identifiers: chr3:g.87311193_87311207del (hg19) ; chr3:g.87262043_87262057del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262047_87262061del , CM000665.2:g.87262047_87262061del	GRCh38
NC_000003.11:g.87311197_87311211del , CM000665.1:g.87311197_87311211del	GRCh37
NC_000003.10:g.87393887_87393901del	NCBI36
NG_008225.2:g.19531_19545del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.682+14_682+28del	ENSP00000342931.3:n.682+14_682+28del
ENST00000350375.7:c.604+14_604+28del MANE Select	ENSP00000263781.2:n.604+14_604+28del
ENST00000344265.7:c.682+14_682+28del	ENSP00000342931.3:n.682+14_682+28del
ENST00000350375.6:c.604+14_604+28del	ENSP00000263781.2:n.604+14_604+28del
ENST00000560656.1:c.440-1953_440-1939del	ENSP00000452610.1:n.440-1953_440-1939del
ENST00000561167.5:c.379+14_379+28del	ENSP00000454072.1:n.379+14_379+28del
NM_000306.3:c.604+14_604+28del	NP_000297.1:n.604+14_604+28del
NM_001122757.2:c.682+14_682+28del	NP_001116229.1:n.682+14_682+28del
NM_000306.4:c.604+14_604+28del MANE Select	NP_000297.1:n.604+14_604+28del
NM_001122757.3:c.682+14_682+28del	NP_001116229.1:n.682+14_682+28del