Canonical Allele Identifier: CA1769083430

Gene: LPL

Linked Data

• dbSNP Id: rs2069808868

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939410_19939435del , CM000670.2:g.19939410_19939435del	GRCh38
NC_000008.10:g.19796921_19796946del , CM000670.1:g.19796921_19796946del	GRCh37
NC_000008.9:g.19841201_19841226del	NCBI36
NG_008855.1:g.5340_5365del
NG_008855.2:g.42694_42719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-31_-6del MANE Select	ENSP00000497642.1:n.-31_-6del
ENST00000311322.8:c.-31_-6del	ENSP00000309757.6:n.-31_-6del
ENST00000519773.1:c.-31_-6del	ENSP00000431028.1:n.-31_-6del
ENST00000520959.5:c.-140-8770_-140-8745del	ENSP00000428496.1:n.-140-8770_-140-8745del
ENST00000521994.1:n.155_180del
ENST00000522701.5:c.-31_-6del	ENSP00000428557.1:n.-31_-6del
ENST00000523696.1:n.39_64del
ENST00000524029.5:c.-31_-6del	ENSP00000428237.1:n.-31_-6del
NM_000237.2:c.-31_-6del	NP_000228.1:n.-31_-6del
NM_000237.3:c.-31_-6del MANE Select	NP_000228.1:n.-31_-6del