Canonical Allele Identifier: CA580154210

Gene: LPL

Linked Data

• dbSNP Id: rs1563561310
• gnomAD v2: 8-19796889-C-CGGCTCA
• gnomAD v3: 8-19939378-C-CGGCTCA
• gnomAD v4: 8-19939378-C-CGGCTCA
• MyVariant Identifiers: chr8:g.19796889_19796890insGGCTCA (hg19) ; chr8:g.19939378_19939379insGGCTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939380_19939385dup , CM000670.2:g.19939380_19939385dup	GRCh38
NC_000008.10:g.19796891_19796896dup , CM000670.1:g.19796891_19796896dup	GRCh37
NC_000008.9:g.19841171_19841176dup	NCBI36
NG_008855.1:g.5310_5315dup
NG_008855.2:g.42664_42669dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-61_-56dup MANE Select	ENSP00000497642.1:n.-61_-56dup
ENST00000311322.8:c.-61_-56dup	ENSP00000309757.6:n.-61_-56dup
ENST00000519773.1:c.-61_-56dup	ENSP00000431028.1:n.-61_-56dup
ENST00000520959.5:c.-140-8800_-140-8795dup	ENSP00000428496.1:n.-140-8800_-140-8795dup
ENST00000521994.1:n.125_130dup
ENST00000522701.5:c.-61_-56dup	ENSP00000428557.1:n.-61_-56dup
ENST00000523696.1:n.9_14dup
ENST00000524029.5:c.-61_-56dup	ENSP00000428237.1:n.-61_-56dup
NM_000237.2:c.-61_-56dup	NP_000228.1:n.-61_-56dup
NM_000237.3:c.-61_-56dup MANE Select	NP_000228.1:n.-61_-56dup