Canonical Allele Identifier: CA1769083321

Gene: LPL

Linked Data

• dbSNP Id: rs2069808033

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939361_19939383del , CM000670.2:g.19939361_19939383del	GRCh38
NC_000008.10:g.19796872_19796894del , CM000670.1:g.19796872_19796894del	GRCh37
NC_000008.9:g.19841152_19841174del	NCBI36
NG_008855.1:g.5291_5313del
NG_008855.2:g.42645_42667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-80_-58del MANE Select	ENSP00000497642.1:n.-80_-58del
ENST00000311322.8:c.-80_-58del	ENSP00000309757.6:n.-80_-58del
ENST00000519773.1:c.-80_-58del	ENSP00000431028.1:n.-80_-58del
ENST00000520959.5:c.-140-8819_-140-8797del	ENSP00000428496.1:n.-140-8819_-140-8797del
ENST00000521994.1:n.106_128del
ENST00000522701.5:c.-80_-58del	ENSP00000428557.1:n.-80_-58del
ENST00000524029.5:c.-80_-58del	ENSP00000428237.1:n.-80_-58del
NM_000237.2:c.-80_-58del	NP_000228.1:n.-80_-58del
NM_000237.3:c.-80_-58del MANE Select	NP_000228.1:n.-80_-58del