Canonical Allele Identifier: CA1769116657
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070094725

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966943del , CM000670.2:g.19966943del GRCh38
NC_000008.10:g.19824454del , CM000670.1:g.19824454del GRCh37
NC_000008.9:g.19868734del NCBI36
NG_008855.1:g.32873del
NG_008855.2:g.70227del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1633del MANE Select ENSP00000497642.1:n.*1633del
ENST00000650478.1:c.2001del ENSP00000497560.1:n.2001del
ENST00000311322.8:c.*1633del ENSP00000309757.6:n.*1633del
NM_000237.2:c.*1633del NP_000228.1:n.*1633del
NM_000237.3:c.*1633del MANE Select NP_000228.1:n.*1633del