Canonical Allele Identifier: CA1769103212

Gene: LPL

Linked Data

• dbSNP Id: rs2069967637

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19954580_19954583dup , CM000670.2:g.19954580_19954583dup	GRCh38
NC_000008.10:g.19812091_19812094dup , CM000670.1:g.19812091_19812094dup	GRCh37
NC_000008.9:g.19856371_19856374dup	NCBI36
NG_008855.1:g.20510_20513dup
NG_008855.2:g.57864_57867dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.775+227_775+230dup MANE Select	ENSP00000497642.1:n.775+227_775+230dup
ENST00000311322.8:c.775+227_775+230dup	ENSP00000309757.6:n.775+227_775+230dup
NM_000237.2:c.775+227_775+230dup	NP_000228.1:n.775+227_775+230dup
NM_000237.3:c.775+227_775+230dup MANE Select	NP_000228.1:n.775+227_775+230dup