Canonical Allele Identifier: CA1769111569
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961713_19961714delinsAG , CM000670.2:g.19961713_19961714delinsAG GRCh38
NC_000008.10:g.19819224_19819225delinsAG , CM000670.1:g.19819224_19819225delinsAG GRCh37
NC_000008.9:g.19863504_19863505delinsAG NCBI36
NG_008855.1:g.27643_27644delinsAG
NG_008855.2:g.64997_64998delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1323-402_1323-401delinsAG MANE Select ENSP00000497642.1:n.1323-402_1323-401delinsAG
ENST00000650478.1:c.263-402_263-401delinsAG ENSP00000497560.1:n.263-402_263-401delinsAG
ENST00000311322.8:c.1323-402_1323-401delinsAG ENSP00000309757.6:n.1323-402_1323-401delinsAG
NM_000237.2:c.1323-402_1323-401delinsAG NP_000228.1:n.1323-402_1323-401delinsAG
NM_000237.3:c.1323-402_1323-401delinsAG MANE Select NP_000228.1:n.1323-402_1323-401delinsAG