Canonical Allele Identifier: CA580154207

Gene: LPL

Linked Data

• dbSNP Id: rs1355753389
• gnomAD v2: 8-19796885-CCTCCGGCTCAG-C
• gnomAD v3: 8-19939374-CCTCCGGCTCAG-C
• gnomAD v4: 8-19939374-CCTCCGGCTCAG-C
• MyVariant Identifiers: chr8:g.19796886_19796896del (hg19) ; chr8:g.19939375_19939385del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939376_19939386del , CM000670.2:g.19939376_19939386del	GRCh38
NC_000008.10:g.19796887_19796897del , CM000670.1:g.19796887_19796897del	GRCh37
NC_000008.9:g.19841167_19841177del	NCBI36
NG_008855.1:g.5306_5316del
NG_008855.2:g.42660_42670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-65_-55del MANE Select	ENSP00000497642.1:n.-65_-55del
ENST00000311322.8:c.-65_-55del	ENSP00000309757.6:n.-65_-55del
ENST00000519773.1:c.-65_-55del	ENSP00000431028.1:n.-65_-55del
ENST00000520959.5:c.-140-8804_-140-8794del	ENSP00000428496.1:n.-140-8804_-140-8794del
ENST00000521994.1:n.121_131del
ENST00000522701.5:c.-65_-55del	ENSP00000428557.1:n.-65_-55del
ENST00000523696.1:n.5_15del
ENST00000524029.5:c.-65_-55del	ENSP00000428237.1:n.-65_-55del
NM_000237.2:c.-65_-55del	NP_000228.1:n.-65_-55del
NM_000237.3:c.-65_-55del MANE Select	NP_000228.1:n.-65_-55del