Canonical Allele Identifier: CA918214962
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1554517888

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958037del , CM000670.2:g.19958037del GRCh38
NC_000008.10:g.19815548del , CM000670.1:g.19815548del GRCh37
NC_000008.9:g.19859828del NCBI36
NG_008855.1:g.23967del
NG_008855.2:g.61321del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1223del MANE Select ENSP00000497642.1:n.1019-1223del
ENST00000650478.1:c.79+1954del ENSP00000497560.1:n.79+1954del
ENST00000311322.8:c.1019-1223del ENSP00000309757.6:n.1019-1223del
NM_000237.2:c.1019-1223del NP_000228.1:n.1019-1223del
NM_000237.3:c.1019-1223del MANE Select NP_000228.1:n.1019-1223del