Canonical Allele Identifier: CA1769107182

Gene: LPL

Linked Data

• dbSNP Id: rs2070002698

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19958026_19958037del , CM000670.2:g.19958026_19958037del	GRCh38
NC_000008.10:g.19815537_19815548del , CM000670.1:g.19815537_19815548del	GRCh37
NC_000008.9:g.19859817_19859828del	NCBI36
NG_008855.1:g.23956_23967del
NG_008855.2:g.61310_61321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1019-1234_1019-1223del MANE Select	ENSP00000497642.1:n.1019-1234_1019-1223del
ENST00000650478.1:c.79+1943_79+1954del	ENSP00000497560.1:n.79+1943_79+1954del
ENST00000311322.8:c.1019-1234_1019-1223del	ENSP00000309757.6:n.1019-1234_1019-1223del
NM_000237.2:c.1019-1234_1019-1223del	NP_000228.1:n.1019-1234_1019-1223del
NM_000237.3:c.1019-1234_1019-1223del MANE Select	NP_000228.1:n.1019-1234_1019-1223del