Canonical Allele Identifier: CA1769102809
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954319_19954320delinsAG , CM000670.2:g.19954319_19954320delinsAG GRCh38
NC_000008.10:g.19811830_19811831delinsAG , CM000670.1:g.19811830_19811831delinsAG GRCh37
NC_000008.9:g.19856110_19856111delinsAG NCBI36
NG_008855.1:g.20249_20250delinsAG
NG_008855.2:g.57603_57604delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.741_742delinsAG MANE Select ENSP00000497642.1:p.Glu247=
ENST00000311322.8:c.741_742delinsAG ENSP00000309757.6:p.Glu247=
NM_000237.2:c.741_742delinsAG NP_000228.1:p.Glu247=
NM_000237.3:c.741_742delinsAG MANE Select NP_000228.1:p.Glu247=
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