Canonical Allele Identifier: CA370467644
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951883C>A , CM000670.2:g.19951883C>A GRCh38
NC_000008.10:g.19809394C>A , CM000670.1:g.19809394C>A GRCh37
NC_000008.9:g.19853674C>A NCBI36
NG_008855.1:g.17813C>A
NG_008855.2:g.55167C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.364C>A MANE Select ENSP00000497642.1:p.Pro122Thr
ENST00000311322.8:c.364C>A ENSP00000309757.6:p.Pro122Thr
ENST00000520959.5:c.136C>A ENSP00000428496.1:p.Pro46Thr
ENST00000524029.5:c.364C>A ENSP00000428237.1:p.Pro122Thr
NM_000237.2:c.364C>A NP_000228.1:p.Pro122Thr
NM_000237.3:c.364C>A MANE Select NP_000228.1:p.Pro122Thr