Canonical Allele Identifier: CA2686362020
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19962021-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962021T>G , CM000670.2:g.19962021T>G GRCh38
NC_000008.10:g.19819532T>G , CM000670.1:g.19819532T>G GRCh37
NC_000008.9:g.19863812T>G NCBI36
NG_008855.1:g.27951T>G
NG_008855.2:g.65305T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1323-94T>G MANE Select ENSP00000497642.1:n.1323-94T>G
ENST00000650478.1:c.263-94T>G ENSP00000497560.1:n.263-94T>G
ENST00000311322.8:c.1323-94T>G ENSP00000309757.6:n.1323-94T>G
NM_000237.2:c.1323-94T>G NP_000228.1:n.1323-94T>G
NM_000237.3:c.1323-94T>G MANE Select NP_000228.1:n.1323-94T>G
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