Canonical Allele Identifier: CA1769083541
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939461C= , CM000670.2:g.19939461C= GRCh38
NC_000008.10:g.19796972C= , CM000670.1:g.19796972C= GRCh37
NC_000008.9:g.19841252C= NCBI36
NG_008855.1:g.5391C=
NG_008855.2:g.42745C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.21C= MANE Select ENSP00000497642.1:p.Leu7=
ENST00000311322.8:c.21C= ENSP00000309757.6:p.Leu7=
ENST00000519773.1:c.21C= ENSP00000431028.1:p.Leu7=
ENST00000520959.5:c.-140-8719C= ENSP00000428496.1:n.-140-8719C=
ENST00000521994.1:n.206C=
ENST00000522701.5:c.21C= ENSP00000428557.1:p.Leu7=
ENST00000523696.1:n.90C=
ENST00000524029.5:c.21C= ENSP00000428237.1:p.Leu7=
NM_000237.2:c.21C= NP_000228.1:p.Leu7=
NM_000237.3:c.21C= MANE Select NP_000228.1:p.Leu7=