Canonical Allele Identifier: CA173376483
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs369297718
MyVariant Identifiers: chr8:g.19809534_19809538del (hg19) chr8:g.19952023_19952027del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952023_19952027del , CM000670.2:g.19952023_19952027del GRCh38
NC_000008.10:g.19809534_19809538del , CM000670.1:g.19809534_19809538del GRCh37
NC_000008.9:g.19853814_19853818del NCBI36
NG_008855.1:g.17953_17957del
NG_008855.2:g.55307_55311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+75_429+79del MANE Select ENSP00000497642.1:n.429+75_429+79del
ENST00000311322.8:c.429+75_429+79del ENSP00000309757.6:n.429+75_429+79del
ENST00000520959.5:c.201+75_201+79del ENSP00000428496.1:n.201+75_201+79del
NM_000237.2:c.429+75_429+79del NP_000228.1:n.429+75_429+79del
NM_000237.3:c.429+75_429+79del MANE Select NP_000228.1:n.429+75_429+79del
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