Canonical Allele Identifier: CA459719156

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19818448A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960937A>T , CM000670.2:g.19960937A>T	GRCh38
NC_000008.10:g.19818448A>T , CM000670.1:g.19818448A>T	GRCh37
NC_000008.9:g.19862728A>T	NCBI36
NG_008855.1:g.26867A>T
NG_008855.2:g.64221A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1176A>T MANE Select	ENSP00000497642.1:p.Leu392=
ENST00000650478.1:c.116A>T	ENSP00000497560.1:p.Ter39Leu
ENST00000311322.8:c.1176A>T	ENSP00000309757.6:p.Leu392=
NM_000237.2:c.1176A>T	NP_000228.1:p.Leu392=
NM_000237.3:c.1176A>T MANE Select	NP_000228.1:p.Leu392=