Canonical Allele Identifier: CA370467737
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951931T>A , CM000670.2:g.19951931T>A GRCh38
NC_000008.10:g.19809442T>A , CM000670.1:g.19809442T>A GRCh37
NC_000008.9:g.19853722T>A NCBI36
NG_008855.1:g.17861T>A
NG_008855.2:g.55215T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.412T>A MANE Select ENSP00000497642.1:p.Phe138Ile
ENST00000311322.8:c.412T>A ENSP00000309757.6:p.Phe138Ile
ENST00000520959.5:c.184T>A ENSP00000428496.1:p.Phe62Ile
NM_000237.2:c.412T>A NP_000228.1:p.Phe138Ile
NM_000237.3:c.412T>A MANE Select NP_000228.1:p.Phe138Ile