Canonical Allele Identifier: CA2695208930
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954202del , CM000670.2:g.19954202del GRCh38
NC_000008.10:g.19811713del , CM000670.1:g.19811713del GRCh37
NC_000008.9:g.19855993del NCBI36
NG_008855.1:g.20132del
NG_008855.2:g.57486del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.624del MANE Select ENSP00000497642.1:p.Leu209TyrfsTer?
ENST00000311322.8:c.624del ENSP00000309757.6:p.Leu209TyrfsTer?
NM_000237.2:c.624del NP_000228.1:p.Leu209TyrfsTer?
NM_000237.3:c.624del MANE Select NP_000228.1:p.Leu209TyrfsTer?