Canonical Allele Identifier: CA2579105736
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939463_19939470dup , CM000670.2:g.19939463_19939470dup GRCh38
NC_000008.10:g.19796974_19796981dup , CM000670.1:g.19796974_19796981dup GRCh37
NC_000008.9:g.19841254_19841261dup NCBI36
NG_008855.1:g.5393_5400dup
NG_008855.2:g.42747_42754dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.23_30dup MANE Select ENSP00000497642.1:p.Leu11CysfsTer2
ENST00000311322.8:c.23_30dup ENSP00000309757.6:p.Leu11CysfsTer2
ENST00000519773.1:c.23_30dup ENSP00000431028.1:p.Leu11CysfsTer2
ENST00000520959.5:c.-140-8717_-140-8710dup ENSP00000428496.1:n.-140-8717_-140-8710dup
ENST00000521994.1:n.208_215dup
ENST00000522701.5:c.23_30dup ENSP00000428557.1:p.Leu11CysfsTer2
ENST00000523696.1:n.92_99dup
ENST00000524029.5:c.23_30dup ENSP00000428237.1:p.Leu11CysfsTer2
NM_000237.2:c.23_30dup NP_000228.1:p.Leu11CysfsTer2
NM_000237.3:c.23_30dup MANE Select NP_000228.1:p.Leu11CysfsTer2