Canonical Allele Identifier: CA1769116849

Gene: LPL

Linked Data

• dbSNP Id: rs2070096354
• gnomAD v3: 8-19967114-A-AGT
• gnomAD v4: 8-19967114-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19967114_19967115insGT , CM000670.2:g.19967114_19967115insGT	GRCh38
NC_000008.10:g.19824625_19824626insGT , CM000670.1:g.19824625_19824626insGT	GRCh37
NC_000008.9:g.19868905_19868906insGT	NCBI36
NG_008855.1:g.33044_33045insGT
NG_008855.2:g.70398_70399insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.*1804_*1805insGT MANE Select	ENSP00000497642.1:n.*1804_*1805insGT
ENST00000650478.1:c.2172_2173insGT	ENSP00000497560.1:n.2172_2173insGT
ENST00000311322.8:c.*1804_*1805insGT	ENSP00000309757.6:n.*1804_*1805insGT
NM_000237.2:c.*1804_*1805insGT	NP_000228.1:n.*1804_*1805insGT
NM_000237.3:c.*1804_*1805insGT MANE Select	NP_000228.1:n.*1804_*1805insGT