Canonical Allele Identifier: CA370638608
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960945C>G , CM000670.2:g.19960945C>G GRCh38
NC_000008.10:g.19818456C>G , CM000670.1:g.19818456C>G GRCh37
NC_000008.9:g.19862736C>G NCBI36
NG_008855.1:g.26875C>G
NG_008855.2:g.64229C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1184C>G MANE Select ENSP00000497642.1:p.Thr395Arg
ENST00000650478.1:c.124C>G ENSP00000497560.1:n.124C>G
ENST00000311322.8:c.1184C>G ENSP00000309757.6:p.Thr395Arg
NM_000237.2:c.1184C>G NP_000228.1:p.Thr395Arg
NM_000237.3:c.1184C>G MANE Select NP_000228.1:p.Thr395Arg