Canonical Allele Identifier: CA2686361440

Gene: LPL

Linked Data

• dbSNP Id: rs2128839557
• gnomAD v4: 8-19960843-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960849del , CM000670.2:g.19960849del	GRCh38
NC_000008.10:g.19818360del , CM000670.1:g.19818360del	GRCh37
NC_000008.9:g.19862640del	NCBI36
NG_008855.1:g.26779del
NG_008855.2:g.64133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1140-52del MANE Select	ENSP00000497642.1:n.1140-52del
ENST00000650478.1:c.80-52del	ENSP00000497560.1:n.80-52del
ENST00000311322.8:c.1140-52del	ENSP00000309757.6:n.1140-52del
NM_000237.2:c.1140-52del	NP_000228.1:n.1140-52del
NM_000237.3:c.1140-52del MANE Select	NP_000228.1:n.1140-52del