Canonical Allele Identifier: CA1769097728
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951852G= , CM000670.2:g.19951852G= GRCh38
NC_000008.10:g.19809363G= , CM000670.1:g.19809363G= GRCh37
NC_000008.9:g.19853643G= NCBI36
NG_008855.1:g.17782G=
NG_008855.2:g.55136G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.333G= MANE Select ENSP00000497642.1:p.Val111=
ENST00000311322.8:c.333G= ENSP00000309757.6:p.Val111=
ENST00000520959.5:c.105G= ENSP00000428496.1:p.Val35=
ENST00000524029.5:c.333G= ENSP00000428237.1:p.Val111=
NM_000237.2:c.333G= NP_000228.1:p.Val111=
NM_000237.3:c.333G= MANE Select NP_000228.1:p.Val111=