Canonical Allele Identifier: CA370467717
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951919G>A , CM000670.2:g.19951919G>A GRCh38
NC_000008.10:g.19809430G>A , CM000670.1:g.19809430G>A GRCh37
NC_000008.9:g.19853710G>A NCBI36
NG_008855.1:g.17849G>A
NG_008855.2:g.55203G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.400G>A MANE Select ENSP00000497642.1:p.Asp134Asn
ENST00000311322.8:c.400G>A ENSP00000309757.6:p.Asp134Asn
ENST00000520959.5:c.172G>A ENSP00000428496.1:p.Asp58Asn
NM_000237.2:c.400G>A NP_000228.1:p.Asp134Asn
NM_000237.3:c.400G>A MANE Select NP_000228.1:p.Asp134Asn