Canonical Allele Identifier: CA459678460
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19809309del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951801del , CM000670.2:g.19951801del GRCh38
NC_000008.10:g.19809312del , CM000670.1:g.19809312del GRCh37
NC_000008.9:g.19853592del NCBI36
NG_008855.1:g.17731del
NG_008855.2:g.55085del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.282del MANE Select ENSP00000497642.1:p.Lys94AsnfsTer?
ENST00000311322.8:c.282del ENSP00000309757.6:p.Lys94AsnfsTer?
ENST00000520959.5:c.54del ENSP00000428496.1:p.Lys18AsnfsTer?
ENST00000521994.1:n.539del
ENST00000522701.5:c.282del ENSP00000428557.1:p.Lys94AsnfsTer?
ENST00000524029.5:c.282del ENSP00000428237.1:p.Lys94AsnfsTer?
NM_000237.2:c.282del NP_000228.1:p.Lys94AsnfsTer?
NM_000237.3:c.282del MANE Select NP_000228.1:p.Lys94AsnfsTer?