Canonical Allele Identifier: CA370464623
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939459C>G , CM000670.2:g.19939459C>G GRCh38
NC_000008.10:g.19796970C>G , CM000670.1:g.19796970C>G GRCh37
NC_000008.9:g.19841250C>G NCBI36
NG_008855.1:g.5389C>G
NG_008855.2:g.42743C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.19C>G MANE Select ENSP00000497642.1:p.Leu7Val
ENST00000311322.8:c.19C>G ENSP00000309757.6:p.Leu7Val
ENST00000519773.1:c.19C>G ENSP00000431028.1:p.Leu7Val
ENST00000520959.5:c.-140-8721C>G ENSP00000428496.1:n.-140-8721C>G
ENST00000521994.1:n.204C>G
ENST00000522701.5:c.19C>G ENSP00000428557.1:p.Leu7Val
ENST00000523696.1:n.88C>G
ENST00000524029.5:c.19C>G ENSP00000428237.1:p.Leu7Val
NM_000237.2:c.19C>G NP_000228.1:p.Leu7Val
NM_000237.3:c.19C>G MANE Select NP_000228.1:p.Leu7Val