Canonical Allele Identifier: CA849558810
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1195784395

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953957A>G , CM000670.2:g.19953957A>G GRCh38
NC_000008.10:g.19811468A>G , CM000670.1:g.19811468A>G GRCh37
NC_000008.9:g.19855748A>G NCBI36
NG_008855.1:g.19887A>G
NG_008855.2:g.57241A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-163A>G MANE Select ENSP00000497642.1:n.542-163A>G
ENST00000311322.8:c.542-163A>G ENSP00000309757.6:n.542-163A>G
ENST00000520959.5:c.314-163A>G ENSP00000428496.1:n.314-163A>G
NM_000237.2:c.542-163A>G NP_000228.1:n.542-163A>G
NM_000237.3:c.542-163A>G MANE Select NP_000228.1:n.542-163A>G