Canonical Allele Identifier: CA370467436

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809313C>G (hg19) ; chr8:g.19951802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951802C>G , CM000670.2:g.19951802C>G	GRCh38
NC_000008.10:g.19809313C>G , CM000670.1:g.19809313C>G	GRCh37
NC_000008.9:g.19853593C>G	NCBI36
NG_008855.1:g.17732C>G
NG_008855.2:g.55086C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.283C>G MANE Select	ENSP00000497642.1:p.Leu95Val
ENST00000311322.8:c.283C>G	ENSP00000309757.6:p.Leu95Val
ENST00000520959.5:c.55C>G	ENSP00000428496.1:p.Leu19Val
ENST00000521994.1:n.540C>G
ENST00000522701.5:c.283C>G	ENSP00000428557.1:p.Leu95Val
ENST00000524029.5:c.283C>G	ENSP00000428237.1:p.Leu95Val
NM_000237.2:c.283C>G	NP_000228.1:p.Leu95Val
NM_000237.3:c.283C>G MANE Select	NP_000228.1:p.Leu95Val