Canonical Allele Identifier: CA1769083510
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939446G= , CM000670.2:g.19939446G= GRCh38
NC_000008.10:g.19796957G= , CM000670.1:g.19796957G= GRCh37
NC_000008.9:g.19841237G= NCBI36
NG_008855.1:g.5376G=
NG_008855.2:g.42730G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.6G= MANE Select ENSP00000497642.1:p.Glu2=
ENST00000311322.8:c.6G= ENSP00000309757.6:p.Glu2=
ENST00000519773.1:c.6G= ENSP00000431028.1:p.Glu2=
ENST00000520959.5:c.-140-8734G= ENSP00000428496.1:n.-140-8734G=
ENST00000521994.1:n.191G=
ENST00000522701.5:c.6G= ENSP00000428557.1:p.Glu2=
ENST00000523696.1:n.75G=
ENST00000524029.5:c.6G= ENSP00000428237.1:p.Glu2=
NM_000237.2:c.6G= NP_000228.1:p.Glu2=
NM_000237.3:c.6G= MANE Select NP_000228.1:p.Glu2=