Canonical Allele Identifier: CA1769116822
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967102T= , CM000670.2:g.19967102T= GRCh38
NC_000008.10:g.19824613T= , CM000670.1:g.19824613T= GRCh37
NC_000008.9:g.19868893T= NCBI36
NG_008855.1:g.33032T=
NG_008855.2:g.70386T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1792T= MANE Select ENSP00000497642.1:n.*1792T=
ENST00000650478.1:c.2160T= ENSP00000497560.1:n.2160T=
ENST00000311322.8:c.*1792T= ENSP00000309757.6:n.*1792T=
NM_000237.2:c.*1792T= NP_000228.1:n.*1792T=
NM_000237.3:c.*1792T= MANE Select NP_000228.1:n.*1792T=
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