Canonical Allele Identifier: CA1769111542
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs324

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961706_19961713del , CM000670.2:g.19961706_19961713del GRCh38
NC_000008.10:g.19819217_19819224del , CM000670.1:g.19819217_19819224del GRCh37
NC_000008.9:g.19863497_19863504del NCBI36
NG_008855.1:g.27636_27643del
NG_008855.2:g.64990_64997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1323-409_1323-402del MANE Select ENSP00000497642.1:n.1323-409_1323-402del
ENST00000650478.1:c.263-409_263-402del ENSP00000497560.1:n.263-409_263-402del
ENST00000311322.8:c.1323-409_1323-402del ENSP00000309757.6:n.1323-409_1323-402del
NM_000237.2:c.1323-409_1323-402del NP_000228.1:n.1323-409_1323-402del
NM_000237.3:c.1323-409_1323-402del MANE Select NP_000228.1:n.1323-409_1323-402del