Canonical Allele Identifier: CA370467572
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069937128

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951850G>A , CM000670.2:g.19951850G>A GRCh38
NC_000008.10:g.19809361G>A , CM000670.1:g.19809361G>A GRCh37
NC_000008.9:g.19853641G>A NCBI36
NG_008855.1:g.17780G>A
NG_008855.2:g.55134G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.331G>A MANE Select ENSP00000497642.1:p.Val111Met
ENST00000311322.8:c.331G>A ENSP00000309757.6:p.Val111Met
ENST00000520959.5:c.103G>A ENSP00000428496.1:p.Val35Met
ENST00000524029.5:c.331G>A ENSP00000428237.1:p.Val111Met
NM_000237.2:c.331G>A NP_000228.1:p.Val111Met
NM_000237.3:c.331G>A MANE Select NP_000228.1:p.Val111Met