Canonical Allele Identifier: CA1111553120
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069996536

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957518_19957521del , CM000670.2:g.19957518_19957521del GRCh38
NC_000008.10:g.19815029_19815032del , CM000670.1:g.19815029_19815032del GRCh37
NC_000008.9:g.19859309_19859312del NCBI36
NG_008855.1:g.23448_23451del
NG_008855.2:g.60802_60805del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1435_1018+1438del MANE Select ENSP00000497642.1:n.1018+1435_1018+1438de...
ENST00000650478.1:c.79+1435_79+1438del ENSP00000497560.1:n.79+1435_79+1438del
ENST00000311322.8:c.1018+1435_1018+1438del ENSP00000309757.6:n.1018+1435_1018+1438de...
NM_000237.2:c.1018+1435_1018+1438del NP_000228.1:n.1018+1435_1018+1438del
NM_000237.3:c.1018+1435_1018+1438del MANE Select NP_000228.1:n.1018+1435_1018+1438del