Canonical Allele Identifier: CA4655650
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs767069210
ExAC: 8:19818379 ATAAC / A
gnomAD v2: 8-19818379-ATAAC-A
gnomAD v3: 8-19960868-ATAAC-A
gnomAD v4: 8-19960868-ATAAC-A
MyVariant Identifiers: chr8:g.19818380_19818383del (hg19) chr8:g.19960870_19960873del (hg38) chr8:g.19960869_19960872del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960873_19960876del , CM000670.2:g.19960873_19960876del GRCh38
NC_000008.10:g.19818384_19818387del , CM000670.1:g.19818384_19818387del GRCh37
NC_000008.9:g.19862664_19862667del NCBI36
NG_008855.1:g.26803_26806del
NG_008855.2:g.64157_64160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-28_1140-25del MANE Select ENSP00000497642.1:n.1140-28_1140-25del
ENST00000650478.1:c.80-28_80-25del ENSP00000497560.1:n.80-28_80-25del
ENST00000311322.8:c.1140-28_1140-25del ENSP00000309757.6:n.1140-28_1140-25del
NM_000237.2:c.1140-28_1140-25del NP_000228.1:n.1140-28_1140-25del
NM_000237.3:c.1140-28_1140-25del MANE Select NP_000228.1:n.1140-28_1140-25del
Search 100 bp 5'
Search 100 bp 3'