Canonical Allele Identifier: CA849561489
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1169434566

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957641del , CM000670.2:g.19957641del GRCh38
NC_000008.10:g.19815152del , CM000670.1:g.19815152del GRCh37
NC_000008.9:g.19859432del NCBI36
NG_008855.1:g.23571del
NG_008855.2:g.60925del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1558del MANE Select ENSP00000497642.1:p.=
ENST00000650478.1:n.79+1558del ENSP00000497560.1:p.=
ENST00000311322.8:c.1018+1558del ENSP00000309757.6:p.=
NM_000237.2:c.1018+1558del NP_000228.1:p.=
NM_000237.3:c.1018+1558del MANE Select NP_000228.1:p.=