Canonical Allele Identifier: CA2686357462
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939424del , CM000670.2:g.19939424del GRCh38
NC_000008.10:g.19796935del , CM000670.1:g.19796935del GRCh37
NC_000008.9:g.19841215del NCBI36
NG_008855.1:g.5354del
NG_008855.2:g.42708del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-17del MANE Select ENSP00000497642.1:n.-17del
ENST00000311322.8:c.-17del ENSP00000309757.6:n.-17del
ENST00000519773.1:c.-17del ENSP00000431028.1:n.-17del
ENST00000520959.5:c.-140-8756del ENSP00000428496.1:n.-140-8756del
ENST00000521994.1:n.169del
ENST00000522701.5:c.-17del ENSP00000428557.1:n.-17del
ENST00000523696.1:n.53del
ENST00000524029.5:c.-17del ENSP00000428237.1:n.-17del
NM_000237.2:c.-17del NP_000228.1:n.-17del
NM_000237.3:c.-17del MANE Select NP_000228.1:n.-17del