Canonical Allele Identifier: CA2686364531
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19966621-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966621C>T , CM000670.2:g.19966621C>T GRCh38
NC_000008.10:g.19824132C>T , CM000670.1:g.19824132C>T GRCh37
NC_000008.9:g.19868412C>T NCBI36
NG_008855.1:g.32551C>T
NG_008855.2:g.69905C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1311C>T MANE Select ENSP00000497642.1:n.*1311C>T
ENST00000650478.1:c.1679C>T ENSP00000497560.1:n.1679C>T
ENST00000311322.8:c.*1311C>T ENSP00000309757.6:n.*1311C>T
NM_000237.2:c.*1311C>T NP_000228.1:n.*1311C>T
NM_000237.3:c.*1311C>T MANE Select NP_000228.1:n.*1311C>T
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