Canonical Allele Identifier: CA2739279728

Gene: LPL

Linked Data

• ClinVar Variation Id: 2845491
• ClinVar RCV Id: RCV003687449

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19948171C>G , CM000670.2:g.19948171C>G	GRCh38
NC_000008.10:g.19805682C>G , CM000670.1:g.19805682C>G	GRCh37
NC_000008.9:g.19849962C>G	NCBI36
NG_008855.1:g.14101C>G
NG_008855.2:g.51455C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.89-9C>G MANE Select	ENSP00000497642.1:n.89-9C>G
ENST00000311322.8:c.89-9C>G	ENSP00000309757.6:n.89-9C>G
ENST00000519773.1:c.*126-9C>G	ENSP00000431028.1:n.*126-9C>G
ENST00000520959.5:c.-140-9C>G	ENSP00000428496.1:n.-140-9C>G
ENST00000521994.1:n.274-9C>G
ENST00000522701.5:c.89-9C>G	ENSP00000428557.1:n.89-9C>G
ENST00000523696.1:n.158-9C>G
ENST00000524029.5:c.89-9C>G	ENSP00000428237.1:n.89-9C>G
NM_000237.2:c.89-9C>G	NP_000228.1:n.89-9C>G
NM_000237.3:c.89-9C>G MANE Select	NP_000228.1:n.89-9C>G