Canonical Allele Identifier: CA4655406
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs780442035
ExAC: 8:19809467 TG / T
gnomAD v2: 8-19809467-TG-T
gnomAD v4: 8-19951956-TG-T
MyVariant Identifiers: chr8:g.19809468del (hg19) chr8:g.19951957del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951959del , CM000670.2:g.19951959del GRCh38
NC_000008.10:g.19809470del , CM000670.1:g.19809470del GRCh37
NC_000008.9:g.19853750del NCBI36
NG_008855.1:g.17889del
NG_008855.2:g.55243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+11del MANE Select ENSP00000497642.1:n.429+11del
ENST00000311322.8:c.429+11del ENSP00000309757.6:n.429+11del
ENST00000520959.5:c.201+11del ENSP00000428496.1:n.201+11del
NM_000237.2:c.429+11del NP_000228.1:n.429+11del
NM_000237.3:c.429+11del MANE Select NP_000228.1:n.429+11del
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Search 100 bp 3'