Canonical Allele Identifier: CA2686357423
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939385_19939393del , CM000670.2:g.19939385_19939393del GRCh38
NC_000008.10:g.19796896_19796904del , CM000670.1:g.19796896_19796904del GRCh37
NC_000008.9:g.19841176_19841184del NCBI36
NG_008855.1:g.5315_5323del
NG_008855.2:g.42669_42677del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-56_-48del MANE Select ENSP00000497642.1:n.-56_-48del
ENST00000311322.8:c.-56_-48del ENSP00000309757.6:n.-56_-48del
ENST00000519773.1:c.-56_-48del ENSP00000431028.1:n.-56_-48del
ENST00000520959.5:c.-140-8795_-140-8787del ENSP00000428496.1:n.-140-8795_-140-8787del
ENST00000521994.1:n.130_138del
ENST00000522701.5:c.-56_-48del ENSP00000428557.1:n.-56_-48del
ENST00000523696.1:n.14_22del
ENST00000524029.5:c.-56_-48del ENSP00000428237.1:n.-56_-48del
NM_000237.2:c.-56_-48del NP_000228.1:n.-56_-48del
NM_000237.3:c.-56_-48del MANE Select NP_000228.1:n.-56_-48del