Canonical Allele Identifier: CA2686357395
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939348_19939356del , CM000670.2:g.19939348_19939356del GRCh38
NC_000008.10:g.19796859_19796867del , CM000670.1:g.19796859_19796867del GRCh37
NC_000008.9:g.19841139_19841147del NCBI36
NG_008855.1:g.5278_5286del
NG_008855.2:g.42632_42640del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-93_-85del MANE Select ENSP00000497642.1:n.-93_-85del
ENST00000311322.8:c.-93_-85del ENSP00000309757.6:n.-93_-85del
ENST00000519773.1:c.-93_-85del ENSP00000431028.1:n.-93_-85del
ENST00000520959.5:c.-140-8832_-140-8824del ENSP00000428496.1:n.-140-8832_-140-8824del
ENST00000521994.1:n.93_101del
ENST00000522701.5:c.-93_-85del ENSP00000428557.1:n.-93_-85del
ENST00000524029.5:c.-93_-85del ENSP00000428237.1:n.-93_-85del
NM_000237.2:c.-93_-85del NP_000228.1:n.-93_-85del
NM_000237.3:c.-93_-85del MANE Select NP_000228.1:n.-93_-85del