Canonical Allele Identifier: CA2779304345
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962848del , CM000670.2:g.19962848del GRCh38
NC_000008.10:g.19820359del , CM000670.1:g.19820359del GRCh37
NC_000008.9:g.19864639del NCBI36
NG_008855.1:g.28778del
NG_008855.2:g.66132del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1427+629del MANE Select ENSP00000497642.1:n.1427+629del
ENST00000650478.1:c.367+629del ENSP00000497560.1:n.367+629del
ENST00000311322.8:c.1427+629del ENSP00000309757.6:n.1427+629del
NM_000237.2:c.1427+629del NP_000228.1:n.1427+629del
NM_000237.3:c.1427+629del MANE Select NP_000228.1:n.1427+629del