Canonical Allele Identifier: CA2686357398
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939354_19939366del , CM000670.2:g.19939354_19939366del GRCh38
NC_000008.10:g.19796865_19796877del , CM000670.1:g.19796865_19796877del GRCh37
NC_000008.9:g.19841145_19841157del NCBI36
NG_008855.1:g.5284_5296del
NG_008855.2:g.42638_42650del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-87_-75del MANE Select ENSP00000497642.1:n.-87_-75del
ENST00000311322.8:c.-87_-75del ENSP00000309757.6:n.-87_-75del
ENST00000519773.1:c.-87_-75del ENSP00000431028.1:n.-87_-75del
ENST00000520959.5:c.-140-8826_-140-8814del ENSP00000428496.1:n.-140-8826_-140-8814del
ENST00000521994.1:n.99_111del
ENST00000522701.5:c.-87_-75del ENSP00000428557.1:n.-87_-75del
ENST00000524029.5:c.-87_-75del ENSP00000428237.1:n.-87_-75del
NM_000237.2:c.-87_-75del NP_000228.1:n.-87_-75del
NM_000237.3:c.-87_-75del MANE Select NP_000228.1:n.-87_-75del