Canonical Allele Identifier: CA1769098207
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1760778162
gnomAD v4: 8-19952068-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952070del , CM000670.2:g.19952070del GRCh38
NC_000008.10:g.19809581del , CM000670.1:g.19809581del GRCh37
NC_000008.9:g.19853861del NCBI36
NG_008855.1:g.18000del
NG_008855.2:g.55354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+122del MANE Select ENSP00000497642.1:n.429+122del
ENST00000311322.8:c.429+122del ENSP00000309757.6:n.429+122del
ENST00000520959.5:c.201+122del ENSP00000428496.1:n.201+122del
NM_000237.2:c.429+122del NP_000228.1:n.429+122del
NM_000237.3:c.429+122del MANE Select NP_000228.1:n.429+122del
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