Canonical Allele Identifier: CA2686360129

Gene: LPL

Linked Data

• gnomAD v4: 8-19951727-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951727G>A , CM000670.2:g.19951727G>A	GRCh38
NC_000008.10:g.19809238G>A , CM000670.1:g.19809238G>A	GRCh37
NC_000008.9:g.19853518G>A	NCBI36
NG_008855.1:g.17657G>A
NG_008855.2:g.55011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.250-42G>A MANE Select	ENSP00000497642.1:n.250-42G>A
ENST00000311322.8:c.250-42G>A	ENSP00000309757.6:n.250-42G>A
ENST00000520959.5:c.22-42G>A	ENSP00000428496.1:n.22-42G>A
ENST00000521994.1:n.465G>A
ENST00000522701.5:c.250-42G>A	ENSP00000428557.1:n.250-42G>A
ENST00000524029.5:c.250-42G>A	ENSP00000428237.1:n.250-42G>A
NM_000237.2:c.250-42G>A	NP_000228.1:n.250-42G>A
NM_000237.3:c.250-42G>A MANE Select	NP_000228.1:n.250-42G>A