Canonical Allele Identifier: CA459678513

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809381T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951870T>A , CM000670.2:g.19951870T>A	GRCh38
NC_000008.10:g.19809381T>A , CM000670.1:g.19809381T>A	GRCh37
NC_000008.9:g.19853661T>A	NCBI36
NG_008855.1:g.17800T>A
NG_008855.2:g.55154T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.351T>A MANE Select	ENSP00000497642.1:p.Ala117=
ENST00000311322.8:c.351T>A	ENSP00000309757.6:p.Ala117=
ENST00000520959.5:c.123T>A	ENSP00000428496.1:p.Ala41=
ENST00000524029.5:c.351T>A	ENSP00000428237.1:p.Ala117=
NM_000237.2:c.351T>A	NP_000228.1:p.Ala117=
NM_000237.3:c.351T>A MANE Select	NP_000228.1:p.Ala117=