Canonical Allele Identifier: CA2686364578
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19966810-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966810A>G , CM000670.2:g.19966810A>G GRCh38
NC_000008.10:g.19824321A>G , CM000670.1:g.19824321A>G GRCh37
NC_000008.9:g.19868601A>G NCBI36
NG_008855.1:g.32740A>G
NG_008855.2:g.70094A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1500A>G MANE Select ENSP00000497642.1:n.*1500A>G
ENST00000650478.1:c.1868A>G ENSP00000497560.1:n.1868A>G
ENST00000311322.8:c.*1500A>G ENSP00000309757.6:n.*1500A>G
NM_000237.2:c.*1500A>G NP_000228.1:n.*1500A>G
NM_000237.3:c.*1500A>G MANE Select NP_000228.1:n.*1500A>G
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