Canonical Allele Identifier: CA849557685

Gene: LPL

Linked Data

• dbSNP Id: rs1053449371
• MyVariant Identifiers: chr8:g.19809700C>T (hg19) ; chr8:g.19952189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19952189C>T , CM000670.2:g.19952189C>T	GRCh38
NC_000008.10:g.19809700C>T , CM000670.1:g.19809700C>T	GRCh37
NC_000008.9:g.19853980C>T	NCBI36
NG_008855.1:g.18119C>T
NG_008855.2:g.55473C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.429+241C>T MANE Select	ENSP00000497642.1:n.429+241C>T
ENST00000311322.8:c.429+241C>T	ENSP00000309757.6:n.429+241C>T
ENST00000520959.5:c.201+241C>T	ENSP00000428496.1:n.201+241C>T
NM_000237.2:c.429+241C>T	NP_000228.1:n.429+241C>T
NM_000237.3:c.429+241C>T MANE Select	NP_000228.1:n.429+241C>T