Canonical Allele Identifier: CA2740920764
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957866T>A , CM000670.2:g.19957866T>A GRCh38
NC_000008.10:g.19815377T>A , CM000670.1:g.19815377T>A GRCh37
NC_000008.9:g.19859657T>A NCBI36
NG_008855.1:g.23796T>A
NG_008855.2:g.61150T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1394T>A MANE Select ENSP00000497642.1:n.1019-1394T>A
ENST00000650478.1:c.79+1783T>A ENSP00000497560.1:n.79+1783T>A
ENST00000311322.8:c.1019-1394T>A ENSP00000309757.6:n.1019-1394T>A
NM_000237.2:c.1019-1394T>A NP_000228.1:n.1019-1394T>A
NM_000237.3:c.1019-1394T>A MANE Select NP_000228.1:n.1019-1394T>A