Canonical Allele Identifier: CA1111569196
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069807763
gnomAD v3: 8-19939336-CT-C
gnomAD v4: 8-19939336-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939338del , CM000670.2:g.19939338del GRCh38
NC_000008.10:g.19796849del , CM000670.1:g.19796849del GRCh37
NC_000008.9:g.19841129del NCBI36
NG_008855.1:g.5268del
NG_008855.2:g.42622del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-103del MANE Select ENSP00000497642.1:n.-103del
ENST00000311322.8:c.-103del ENSP00000309757.6:n.-103del
ENST00000519773.1:c.-103del ENSP00000431028.1:n.-103del
ENST00000520959.5:c.-140-8842del ENSP00000428496.1:n.-140-8842del
ENST00000521994.1:n.83del
ENST00000522701.5:c.-103del ENSP00000428557.1:n.-103del
ENST00000524029.5:c.-103del ENSP00000428237.1:n.-103del
NM_000237.2:c.-103del NP_000228.1:n.-103del
NM_000237.3:c.-103del MANE Select NP_000228.1:n.-103del
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