Canonical Allele Identifier: CA1769097071
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951553_19951558delinsCCTCAA , CM000670.2:g.19951553_19951558delinsCCTCAA GRCh38
NC_000008.10:g.19809064_19809069delinsCCTCAA , CM000670.1:g.19809064_19809069delinsCCTCAA GRCh37
NC_000008.9:g.19853344_19853349delinsCCTCAA NCBI36
NG_008855.1:g.17483_17488delinsCCTCAA
NG_008855.2:g.54837_54842delinsCCTCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-216_250-211delinsCCTCAA MANE Select ENSP00000497642.1:n.250-216_250-211delinsCCTCAA
ENST00000311322.8:c.250-216_250-211delinsCCTCAA ENSP00000309757.6:n.250-216_250-211delinsCCTCAA
ENST00000520959.5:c.22-216_22-211delinsCCTCAA ENSP00000428496.1:n.22-216_22-211delinsCCTCAA
ENST00000521994.1:n.435-144_435-139delinsCCTCAA
ENST00000522701.5:c.250-216_250-211delinsCCTCAA ENSP00000428557.1:n.250-216_250-211delinsCCTCAA
ENST00000524029.5:c.250-216_250-211delinsCCTCAA ENSP00000428237.1:n.250-216_250-211delinsCCTCAA
NM_000237.2:c.250-216_250-211delinsCCTCAA NP_000228.1:n.250-216_250-211delinsCCTCAA
NM_000237.3:c.250-216_250-211delinsCCTCAA MANE Select NP_000228.1:n.250-216_250-211delinsCCTCAA