Canonical Allele Identifier: CA1111569222
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069808365
gnomAD v3: 8-19939380-G-A
gnomAD v4: 8-19939380-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939380G>A , CM000670.2:g.19939380G>A GRCh38
NC_000008.10:g.19796891G>A , CM000670.1:g.19796891G>A GRCh37
NC_000008.9:g.19841171G>A NCBI36
NG_008855.1:g.5310G>A
NG_008855.2:g.42664G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-61G>A MANE Select ENSP00000497642.1:n.-61G>A
ENST00000311322.8:c.-61G>A ENSP00000309757.6:n.-61G>A
ENST00000519773.1:c.-61G>A ENSP00000431028.1:n.-61G>A
ENST00000520959.5:c.-140-8800G>A ENSP00000428496.1:n.-140-8800G>A
ENST00000521994.1:n.125G>A
ENST00000522701.5:c.-61G>A ENSP00000428557.1:n.-61G>A
ENST00000523696.1:n.9G>A
ENST00000524029.5:c.-61G>A ENSP00000428237.1:n.-61G>A
NM_000237.2:c.-61G>A NP_000228.1:n.-61G>A
NM_000237.3:c.-61G>A MANE Select NP_000228.1:n.-61G>A
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