Canonical Allele Identifier: CA173370929

Gene: LPL

Linked Data

• dbSNP Id: rs750065070
• MyVariant Identifiers: chr8:g.19796901_19796902del (hg19) ; chr8:g.19939390_19939391del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939391_19939392del , CM000670.2:g.19939391_19939392del	GRCh38
NC_000008.10:g.19796902_19796903del , CM000670.1:g.19796902_19796903del	GRCh37
NC_000008.9:g.19841182_19841183del	NCBI36
NG_008855.1:g.5321_5322del
NG_008855.2:g.42675_42676del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-50_-49del MANE Select	ENSP00000497642.1:n.-50_-49del
ENST00000311322.8:c.-50_-49del	ENSP00000309757.6:n.-50_-49del
ENST00000519773.1:c.-50_-49del	ENSP00000431028.1:n.-50_-49del
ENST00000520959.5:c.-140-8789_-140-8788del	ENSP00000428496.1:n.-140-8789_-140-8788del
ENST00000521994.1:n.136_137del
ENST00000522701.5:c.-50_-49del	ENSP00000428557.1:n.-50_-49del
ENST00000523696.1:n.20_21del
ENST00000524029.5:c.-50_-49del	ENSP00000428237.1:n.-50_-49del
NM_000237.2:c.-50_-49del	NP_000228.1:n.-50_-49del
NM_000237.3:c.-50_-49del MANE Select	NP_000228.1:n.-50_-49del