Canonical Allele Identifier: CA370468599
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954287G>A , CM000670.2:g.19954287G>A GRCh38
NC_000008.10:g.19811798G>A , CM000670.1:g.19811798G>A GRCh37
NC_000008.9:g.19856078G>A NCBI36
NG_008855.1:g.20217G>A
NG_008855.2:g.57571G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.709G>A MANE Select ENSP00000497642.1:p.Gly237Ser
ENST00000311322.8:c.709G>A ENSP00000309757.6:p.Gly237Ser
NM_000237.2:c.709G>A NP_000228.1:p.Gly237Ser
NM_000237.3:c.709G>A MANE Select NP_000228.1:p.Gly237Ser