Canonical Allele Identifier: CA2686360203
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952090_19952092del , CM000670.2:g.19952090_19952092del GRCh38
NC_000008.10:g.19809601_19809603del , CM000670.1:g.19809601_19809603del GRCh37
NC_000008.9:g.19853881_19853883del NCBI36
NG_008855.1:g.18020_18022del
NG_008855.2:g.55374_55376del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+142_429+144del MANE Select ENSP00000497642.1:n.429+142_429+144del
ENST00000311322.8:c.429+142_429+144del ENSP00000309757.6:n.429+142_429+144del
ENST00000520959.5:c.201+142_201+144del ENSP00000428496.1:n.201+142_201+144del
NM_000237.2:c.429+142_429+144del NP_000228.1:n.429+142_429+144del
NM_000237.3:c.429+142_429+144del MANE Select NP_000228.1:n.429+142_429+144del