Canonical Allele Identifier: CA2686357471

Gene: LPL

Linked Data

• gnomAD v4: 8-19939432-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939432C>A , CM000670.2:g.19939432C>A	GRCh38
NC_000008.10:g.19796943C>A , CM000670.1:g.19796943C>A	GRCh37
NC_000008.9:g.19841223C>A	NCBI36
NG_008855.1:g.5362C>A
NG_008855.2:g.42716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-9C>A MANE Select	ENSP00000497642.1:n.-9C>A
ENST00000311322.8:c.-9C>A	ENSP00000309757.6:n.-9C>A
ENST00000519773.1:c.-9C>A	ENSP00000431028.1:n.-9C>A
ENST00000520959.5:c.-140-8748C>A	ENSP00000428496.1:n.-140-8748C>A
ENST00000521994.1:n.177C>A
ENST00000522701.5:c.-9C>A	ENSP00000428557.1:n.-9C>A
ENST00000523696.1:n.61C>A
ENST00000524029.5:c.-9C>A	ENSP00000428237.1:n.-9C>A
NM_000237.2:c.-9C>A	NP_000228.1:n.-9C>A
NM_000237.3:c.-9C>A MANE Select	NP_000228.1:n.-9C>A