Canonical Allele Identifier: CA459678535

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809418C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951907C>T , CM000670.2:g.19951907C>T	GRCh38
NC_000008.10:g.19809418C>T , CM000670.1:g.19809418C>T	GRCh37
NC_000008.9:g.19853698C>T	NCBI36
NG_008855.1:g.17837C>T
NG_008855.2:g.55191C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.388C>T MANE Select	ENSP00000497642.1:p.Leu130=
ENST00000311322.8:c.388C>T	ENSP00000309757.6:p.Leu130=
ENST00000520959.5:c.160C>T	ENSP00000428496.1:p.Leu54=
ENST00000524029.5:c.388C>T
NM_000237.2:c.388C>T	NP_000228.1:p.Leu130=
NM_000237.3:c.388C>T MANE Select	NP_000228.1:p.Leu130=