Canonical Allele Identifier: CA1769083386
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939389_19939391delinsGCT , CM000670.2:g.19939389_19939391delinsGCT GRCh38
NC_000008.10:g.19796900_19796902delinsGCT , CM000670.1:g.19796900_19796902delinsGCT GRCh37
NC_000008.9:g.19841180_19841182delinsGCT NCBI36
NG_008855.1:g.5319_5321delinsGCT
NG_008855.2:g.42673_42675delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-52_-50delinsGCT MANE Select ENSP00000497642.1:n.-52_-50delinsGCT
ENST00000311322.8:c.-52_-50delinsGCT ENSP00000309757.6:n.-52_-50delinsGCT
ENST00000519773.1:c.-52_-50delinsGCT ENSP00000431028.1:n.-52_-50delinsGCT
ENST00000520959.5:c.-140-8791_-140-8789delinsGCT ENSP00000428496.1:n.-140-8791_-140-8789delinsGCT
ENST00000521994.1:n.134_136delinsGCT
ENST00000522701.5:c.-52_-50delinsGCT ENSP00000428557.1:n.-52_-50delinsGCT
ENST00000523696.1:n.18_20delinsGCT
ENST00000524029.5:c.-52_-50delinsGCT ENSP00000428237.1:n.-52_-50delinsGCT
NM_000237.2:c.-52_-50delinsGCT NP_000228.1:n.-52_-50delinsGCT
NM_000237.3:c.-52_-50delinsGCT MANE Select NP_000228.1:n.-52_-50delinsGCT