Canonical Allele Identifier: CA459678556
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19809447C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951936C>A , CM000670.2:g.19951936C>A GRCh38
NC_000008.10:g.19809447C>A , CM000670.1:g.19809447C>A GRCh37
NC_000008.9:g.19853727C>A NCBI36
NG_008855.1:g.17866C>A
NG_008855.2:g.55220C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.417C>A MANE Select ENSP00000497642.1:p.Ile139=
ENST00000311322.8:c.417C>A ENSP00000309757.6:p.Ile139=
ENST00000520959.5:c.189C>A ENSP00000428496.1:p.Ile63=
NM_000237.2:c.417C>A NP_000228.1:p.Ile139=
NM_000237.3:c.417C>A MANE Select NP_000228.1:p.Ile139=