Canonical Allele Identifier: CA370467613
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951871C>G , CM000670.2:g.19951871C>G GRCh38
NC_000008.10:g.19809382C>G , CM000670.1:g.19809382C>G GRCh37
NC_000008.9:g.19853662C>G NCBI36
NG_008855.1:g.17801C>G
NG_008855.2:g.55155C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.352C>G MANE Select ENSP00000497642.1:p.Gln118Glu
ENST00000311322.8:c.352C>G ENSP00000309757.6:p.Gln118Glu
ENST00000520959.5:c.124C>G ENSP00000428496.1:p.Gln42Glu
ENST00000524029.5:c.352C>G ENSP00000428237.1:p.Gln118Glu
NM_000237.2:c.352C>G NP_000228.1:p.Gln118Glu
NM_000237.3:c.352C>G MANE Select NP_000228.1:p.Gln118Glu