Canonical Allele Identifier: CA1769096988

Gene: LPL

Linked Data

• dbSNP Id: rs2069933909

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951512A>G , CM000670.2:g.19951512A>G	GRCh38
NC_000008.10:g.19809023A>G , CM000670.1:g.19809023A>G	GRCh37
NC_000008.9:g.19853303A>G	NCBI36
NG_008855.1:g.17442A>G
NG_008855.2:g.54796A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.250-257A>G MANE Select	ENSP00000497642.1:n.250-257A>G
ENST00000311322.8:c.250-257A>G	ENSP00000309757.6:n.250-257A>G
ENST00000520959.5:c.22-257A>G	ENSP00000428496.1:n.22-257A>G
ENST00000521994.1:n.435-185A>G
ENST00000522701.5:c.250-257A>G	ENSP00000428557.1:n.250-257A>G
ENST00000524029.5:c.250-257A>G	ENSP00000428237.1:n.250-257A>G
NM_000237.2:c.250-257A>G	NP_000228.1:n.250-257A>G
NM_000237.3:c.250-257A>G MANE Select	NP_000228.1:n.250-257A>G