Canonical Allele Identifier: CA1769083537
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939458G= , CM000670.2:g.19939458G= GRCh38
NC_000008.10:g.19796969G= , CM000670.1:g.19796969G= GRCh37
NC_000008.9:g.19841249G= NCBI36
NG_008855.1:g.5388G=
NG_008855.2:g.42742G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.18G= MANE Select ENSP00000497642.1:p.Leu6=
ENST00000311322.8:c.18G= ENSP00000309757.6:p.Leu6=
ENST00000519773.1:c.18G= ENSP00000431028.1:p.Leu6=
ENST00000520959.5:c.-140-8722G= ENSP00000428496.1:n.-140-8722G=
ENST00000521994.1:n.203G=
ENST00000522701.5:c.18G= ENSP00000428557.1:p.Leu6=
ENST00000523696.1:n.87G=
ENST00000524029.5:c.18G= ENSP00000428237.1:p.Leu6=
NM_000237.2:c.18G= NP_000228.1:p.Leu6=
NM_000237.3:c.18G= MANE Select NP_000228.1:p.Leu6=