Canonical Allele Identifier: CA1769110523
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070031419
gnomAD v4: 8-19960819-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960819A>G , CM000670.2:g.19960819A>G GRCh38
NC_000008.10:g.19818330A>G , CM000670.1:g.19818330A>G GRCh37
NC_000008.9:g.19862610A>G NCBI36
NG_008855.1:g.26749A>G
NG_008855.2:g.64103A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1140-82A>G MANE Select ENSP00000497642.1:n.1140-82A>G
ENST00000650478.1:c.80-82A>G ENSP00000497560.1:n.80-82A>G
ENST00000311322.8:c.1140-82A>G ENSP00000309757.6:n.1140-82A>G
NM_000237.2:c.1140-82A>G NP_000228.1:n.1140-82A>G
NM_000237.3:c.1140-82A>G MANE Select NP_000228.1:n.1140-82A>G
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