Canonical Allele Identifier: CA2716564553
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2128839939

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962775A>G , CM000670.2:g.19962775A>G GRCh38
NC_000008.10:g.19820286A>G , CM000670.1:g.19820286A>G GRCh37
NC_000008.9:g.19864566A>G NCBI36
NG_008855.1:g.28705A>G
NG_008855.2:g.66059A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1427+556A>G MANE Select ENSP00000497642.1:n.1427+556A>G
ENST00000650478.1:c.367+556A>G ENSP00000497560.1:n.367+556A>G
ENST00000311322.8:c.1427+556A>G ENSP00000309757.6:n.1427+556A>G
NM_000237.2:c.1427+556A>G NP_000228.1:n.1427+556A>G
NM_000237.3:c.1427+556A>G MANE Select NP_000228.1:n.1427+556A>G