Canonical Allele Identifier: CA370468289
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954138C>A , CM000670.2:g.19954138C>A GRCh38
NC_000008.10:g.19811649C>A , CM000670.1:g.19811649C>A GRCh37
NC_000008.9:g.19855929C>A NCBI36
NG_008855.1:g.20068C>A
NG_008855.2:g.57422C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.560C>A MANE Select ENSP00000497642.1:p.Pro187His
ENST00000311322.8:c.560C>A ENSP00000309757.6:p.Pro187His
ENST00000520959.5:c.332C>A ENSP00000428496.1:p.Pro111His
NM_000237.2:c.560C>A NP_000228.1:p.Pro187His
NM_000237.3:c.560C>A MANE Select NP_000228.1:p.Pro187His