Canonical Allele Identifier: CA1769083378

Gene: LPL

Linked Data

• dbSNP Id: rs2069808440

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939387C>G , CM000670.2:g.19939387C>G	GRCh38
NC_000008.10:g.19796898C>G , CM000670.1:g.19796898C>G	GRCh37
NC_000008.9:g.19841178C>G	NCBI36
NG_008855.1:g.5317C>G
NG_008855.2:g.42671C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-54C>G MANE Select	ENSP00000497642.1:n.-54C>G
ENST00000311322.8:c.-54C>G	ENSP00000309757.6:n.-54C>G
ENST00000519773.1:c.-54C>G	ENSP00000431028.1:n.-54C>G
ENST00000520959.5:c.-140-8793C>G	ENSP00000428496.1:n.-140-8793C>G
ENST00000521994.1:n.132C>G
ENST00000522701.5:c.-54C>G	ENSP00000428557.1:n.-54C>G
ENST00000523696.1:n.16C>G
ENST00000524029.5:c.-54C>G	ENSP00000428237.1:n.-54C>G
NM_000237.2:c.-54C>G	NP_000228.1:n.-54C>G
NM_000237.3:c.-54C>G MANE Select	NP_000228.1:n.-54C>G