Canonical Allele Identifier: CA1769106891
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957798_19957799delinsTA , CM000670.2:g.19957798_19957799delinsTA GRCh38
NC_000008.10:g.19815309_19815310delinsTA , CM000670.1:g.19815309_19815310delinsTA GRCh37
NC_000008.9:g.19859589_19859590delinsTA NCBI36
NG_008855.1:g.23728_23729delinsTA
NG_008855.2:g.61082_61083delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1462_1019-1461delinsTA MANE Select ENSP00000497642.1:n.1019-1462_1019-1461delinsTA
ENST00000650478.1:c.79+1715_79+1716delinsTA ENSP00000497560.1:n.79+1715_79+1716delinsTA
ENST00000311322.8:c.1019-1462_1019-1461delinsTA ENSP00000309757.6:n.1019-1462_1019-1461delinsTA
NM_000237.2:c.1019-1462_1019-1461delinsTA NP_000228.1:n.1019-1462_1019-1461delinsTA
NM_000237.3:c.1019-1462_1019-1461delinsTA MANE Select NP_000228.1:n.1019-1462_1019-1461delinsTA
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