Canonical Allele Identifier: CA2686361387

Gene: LPL

Linked Data

• gnomAD v4: 8-19960752-CATTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960753_19960757del , CM000670.2:g.19960753_19960757del	GRCh38
NC_000008.10:g.19818264_19818268del , CM000670.1:g.19818264_19818268del	GRCh37
NC_000008.9:g.19862544_19862548del	NCBI36
NG_008855.1:g.26683_26687del
NG_008855.2:g.64037_64041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1140-148_1140-144del MANE Select	ENSP00000497642.1:n.1140-148_1140-144del
ENST00000650478.1:c.80-148_80-144del	ENSP00000497560.1:n.80-148_80-144del
ENST00000311322.8:c.1140-148_1140-144del	ENSP00000309757.6:n.1140-148_1140-144del
NM_000237.2:c.1140-148_1140-144del	NP_000228.1:n.1140-148_1140-144del
NM_000237.3:c.1140-148_1140-144del MANE Select	NP_000228.1:n.1140-148_1140-144del