Canonical Allele Identifier: CA2686357385
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939337_19939347del , CM000670.2:g.19939337_19939347del GRCh38
NC_000008.10:g.19796848_19796858del , CM000670.1:g.19796848_19796858del GRCh37
NC_000008.9:g.19841128_19841138del NCBI36
NG_008855.1:g.5267_5277del
NG_008855.2:g.42621_42631del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-104_-94del MANE Select ENSP00000497642.1:n.-104_-94del
ENST00000311322.8:c.-104_-94del ENSP00000309757.6:n.-104_-94del
ENST00000519773.1:c.-104_-94del ENSP00000431028.1:n.-104_-94del
ENST00000520959.5:c.-140-8843_-140-8833del ENSP00000428496.1:n.-140-8843_-140-8833del
ENST00000521994.1:n.82_92del
ENST00000522701.5:c.-104_-94del ENSP00000428557.1:n.-104_-94del
ENST00000524029.5:c.-104_-94del ENSP00000428237.1:n.-104_-94del
NM_000237.2:c.-104_-94del NP_000228.1:n.-104_-94del
NM_000237.3:c.-104_-94del MANE Select NP_000228.1:n.-104_-94del