Canonical Allele Identifier: CA459678508

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809378G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951867G>T , CM000670.2:g.19951867G>T	GRCh38
NC_000008.10:g.19809378G>T , CM000670.1:g.19809378G>T	GRCh37
NC_000008.9:g.19853658G>T	NCBI36
NG_008855.1:g.17797G>T
NG_008855.2:g.55151G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.348G>T MANE Select	ENSP00000497642.1:p.Arg116=
ENST00000311322.8:c.348G>T	ENSP00000309757.6:p.Arg116=
ENST00000520959.5:c.120G>T	ENSP00000428496.1:p.Arg40=
ENST00000524029.5:c.348G>T	ENSP00000428237.1:p.Arg116=
NM_000237.2:c.348G>T	NP_000228.1:p.Arg116=
NM_000237.3:c.348G>T MANE Select	NP_000228.1:p.Arg116=