Canonical Allele Identifier: CA1769106882

Gene: LPL

Linked Data

• dbSNP Id: rs2070000083

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19957792A>G , CM000670.2:g.19957792A>G	GRCh38
NC_000008.10:g.19815303A>G , CM000670.1:g.19815303A>G	GRCh37
NC_000008.9:g.19859583A>G	NCBI36
NG_008855.1:g.23722A>G
NG_008855.2:g.61076A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1019-1468A>G MANE Select	ENSP00000497642.1:n.1019-1468A>G
ENST00000650478.1:c.79+1709A>G	ENSP00000497560.1:n.79+1709A>G
ENST00000311322.8:c.1019-1468A>G	ENSP00000309757.6:n.1019-1468A>G
NM_000237.2:c.1019-1468A>G	NP_000228.1:n.1019-1468A>G
NM_000237.3:c.1019-1468A>G MANE Select	NP_000228.1:n.1019-1468A>G