Canonical Allele Identifier: CA2569608945
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960779del , CM000670.2:g.19960779del GRCh38
NC_000008.10:g.19818290del , CM000670.1:g.19818290del GRCh37
NC_000008.9:g.19862570del NCBI36
NG_008855.1:g.26709del
NG_008855.2:g.64063del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1140-122del MANE Select ENSP00000497642.1:n.1140-122del
ENST00000650478.1:c.80-122del ENSP00000497560.1:n.80-122del
ENST00000311322.8:c.1140-122del ENSP00000309757.6:n.1140-122del
NM_000237.2:c.1140-122del NP_000228.1:n.1140-122del
NM_000237.3:c.1140-122del MANE Select NP_000228.1:n.1140-122del