Canonical Allele Identifier: CA2579105803
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952032C>A , CM000670.2:g.19952032C>A GRCh38
NC_000008.10:g.19809543C>A , CM000670.1:g.19809543C>A GRCh37
NC_000008.9:g.19853823C>A NCBI36
NG_008855.1:g.17962C>A
NG_008855.2:g.55316C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+84C>A MANE Select ENSP00000497642.1:n.429+84C>A
ENST00000311322.8:c.429+84C>A ENSP00000309757.6:n.429+84C>A
ENST00000520959.5:c.201+84C>A ENSP00000428496.1:n.201+84C>A
NM_000237.2:c.429+84C>A NP_000228.1:n.429+84C>A
NM_000237.3:c.429+84C>A MANE Select NP_000228.1:n.429+84C>A
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