Canonical Allele Identifier: CA1139660389
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 909614
ClinVar RCV Id: RCV001160771
dbSNP Id: rs2070094189
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966857T>A , CM000670.2:g.19966857T>A GRCh38
NC_000008.10:g.19824368T>A , CM000670.1:g.19824368T>A GRCh37
NC_000008.9:g.19868648T>A NCBI36
NG_008855.1:g.32787T>A
NG_008855.2:g.70141T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1547T>A MANE Select ENSP00000497642.1:n.*1547T>A
ENST00000650478.1:c.1915T>A ENSP00000497560.1:n.1915T>A
ENST00000311322.8:c.*1547T>A ENSP00000309757.6:n.*1547T>A
NM_000237.2:c.*1547T>A NP_000228.1:n.*1547T>A
NM_000237.3:c.*1547T>A MANE Select NP_000228.1:n.*1547T>A
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