Canonical Allele Identifier: CA849557579
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1472681899
gnomAD v4: 8-19952034-CT-C
MyVariant Identifiers: chr8:g.19809546del (hg19) chr8:g.19952035del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952036del , CM000670.2:g.19952036del GRCh38
NC_000008.10:g.19809547del , CM000670.1:g.19809547del GRCh37
NC_000008.9:g.19853827del NCBI36
NG_008855.1:g.17966del
NG_008855.2:g.55320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+88del MANE Select ENSP00000497642.1:n.429+88del
ENST00000311322.8:c.429+88del ENSP00000309757.6:n.429+88del
ENST00000520959.5:c.201+88del ENSP00000428496.1:n.201+88del
NM_000237.2:c.429+88del NP_000228.1:n.429+88del
NM_000237.3:c.429+88del MANE Select NP_000228.1:n.429+88del
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