Canonical Allele Identifier: CA370638532
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960906A>G , CM000670.2:g.19960906A>G GRCh38
NC_000008.10:g.19818417A>G , CM000670.1:g.19818417A>G GRCh37
NC_000008.9:g.19862697A>G NCBI36
NG_008855.1:g.26836A>G
NG_008855.2:g.64190A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1145A>G MANE Select ENSP00000497642.1:p.Glu382Gly
ENST00000650478.1:c.85A>G ENSP00000497560.1:p.Lys29Glu
ENST00000311322.8:c.1145A>G ENSP00000309757.6:p.Glu382Gly
NM_000237.2:c.1145A>G NP_000228.1:p.Glu382Gly
NM_000237.3:c.1145A>G MANE Select NP_000228.1:p.Glu382Gly