Canonical Allele Identifier: CA459678496

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809360G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951849G>C , CM000670.2:g.19951849G>C	GRCh38
NC_000008.10:g.19809360G>C , CM000670.1:g.19809360G>C	GRCh37
NC_000008.9:g.19853640G>C	NCBI36
NG_008855.1:g.17779G>C
NG_008855.2:g.55133G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.330G>C MANE Select	ENSP00000497642.1:p.Val110=
ENST00000311322.8:c.330G>C	ENSP00000309757.6:p.Val110=
ENST00000520959.5:c.102G>C	ENSP00000428496.1:p.Val34=
ENST00000524029.5:c.330G>C	ENSP00000428237.1:p.Val110=
NM_000237.2:c.330G>C	NP_000228.1:p.Val110=
NM_000237.3:c.330G>C MANE Select	NP_000228.1:p.Val110=