Canonical Allele Identifier: CA459678524
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19809402C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951891C>A , CM000670.2:g.19951891C>A GRCh38
NC_000008.10:g.19809402C>A , CM000670.1:g.19809402C>A GRCh37
NC_000008.9:g.19853682C>A NCBI36
NG_008855.1:g.17821C>A
NG_008855.2:g.55175C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.372C>A MANE Select ENSP00000497642.1:p.Ser124=
ENST00000311322.8:c.372C>A ENSP00000309757.6:p.Ser124=
ENST00000520959.5:c.144C>A ENSP00000428496.1:p.Ser48=
ENST00000524029.5:c.372C>A ENSP00000428237.1:p.Ser124=
NM_000237.2:c.372C>A NP_000228.1:p.Ser124=
NM_000237.3:c.372C>A MANE Select NP_000228.1:p.Ser124=