Canonical Allele Identifier: CA1769098363
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952134G= , CM000670.2:g.19952134G= GRCh38
NC_000008.10:g.19809645G= , CM000670.1:g.19809645G= GRCh37
NC_000008.9:g.19853925G= NCBI36
NG_008855.1:g.18064G=
NG_008855.2:g.55418G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+186G= MANE Select ENSP00000497642.1:n.429+186G=
ENST00000311322.8:c.429+186G= ENSP00000309757.6:n.429+186G=
ENST00000520959.5:c.201+186G= ENSP00000428496.1:n.201+186G=
NM_000237.2:c.429+186G= NP_000228.1:n.429+186G=
NM_000237.3:c.429+186G= MANE Select NP_000228.1:n.429+186G=