Canonical Allele Identifier: CA173618737

Gene: LPL

Linked Data

• dbSNP Id: rs982212336
• MyVariant Identifiers: chr8:g.19824316T>G (hg19) ; chr8:g.19966805T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19966805T>G , CM000670.2:g.19966805T>G	GRCh38
NC_000008.10:g.19824316T>G , CM000670.1:g.19824316T>G	GRCh37
NC_000008.9:g.19868596T>G	NCBI36
NG_008855.1:g.32735T>G
NG_008855.2:g.70089T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.*1495T>G MANE Select	ENSP00000497642.1:n.*1495T>G
ENST00000650478.1:c.1863T>G	ENSP00000497560.1:n.1863T>G
ENST00000311322.8:c.*1495T>G	ENSP00000309757.6:n.*1495T>G
NM_000237.2:c.*1495T>G	NP_000228.1:n.*1495T>G
NM_000237.3:c.*1495T>G MANE Select	NP_000228.1:n.*1495T>G