Canonical Allele Identifier: CA2686360451
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954286del , CM000670.2:g.19954286del GRCh38
NC_000008.10:g.19811797del , CM000670.1:g.19811797del GRCh37
NC_000008.9:g.19856077del NCBI36
NG_008855.1:g.20216del
NG_008855.2:g.57570del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.708del MANE Select ENSP00000497642.1:p.Gly237ValfsTer15
ENST00000311322.8:c.708del ENSP00000309757.6:p.Gly237ValfsTer15
NM_000237.2:c.708del NP_000228.1:p.Gly237ValfsTer15
NM_000237.3:c.708del MANE Select NP_000228.1:p.Gly237ValfsTer15