Canonical Allele Identifier: CA459678490
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19809354C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951843C>A , CM000670.2:g.19951843C>A GRCh38
NC_000008.10:g.19809354C>A , CM000670.1:g.19809354C>A GRCh37
NC_000008.9:g.19853634C>A NCBI36
NG_008855.1:g.17773C>A
NG_008855.2:g.55127C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.324C>A MANE Select ENSP00000497642.1:p.Val108=
ENST00000311322.8:c.324C>A ENSP00000309757.6:p.Val108=
ENST00000520959.5:c.96C>A ENSP00000428496.1:p.Val32=
ENST00000524029.5:c.324C>A ENSP00000428237.1:p.Val108=
NM_000237.2:c.324C>A NP_000228.1:p.Val108=
NM_000237.3:c.324C>A MANE Select NP_000228.1:p.Val108=