Canonical Allele Identifier: CA2686360529
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954505del , CM000670.2:g.19954505del GRCh38
NC_000008.10:g.19812016del , CM000670.1:g.19812016del GRCh37
NC_000008.9:g.19856296del NCBI36
NG_008855.1:g.20435del
NG_008855.2:g.57789del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+152del MANE Select ENSP00000497642.1:n.775+152del
ENST00000311322.8:c.775+152del ENSP00000309757.6:n.775+152del
NM_000237.2:c.775+152del NP_000228.1:n.775+152del
NM_000237.3:c.775+152del MANE Select NP_000228.1:n.775+152del