Canonical Allele Identifier: CA1769106657
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957588_19957591delinsTCAC , CM000670.2:g.19957588_19957591delinsTCAC GRCh38
NC_000008.10:g.19815099_19815102delinsTCAC , CM000670.1:g.19815099_19815102delinsTCAC GRCh37
NC_000008.9:g.19859379_19859382delinsTCAC NCBI36
NG_008855.1:g.23518_23521delinsTCAC
NG_008855.2:g.60872_60875delinsTCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1505_1018+1508delinsTCAC MANE Select ENSP00000497642.1:p.=
ENST00000650478.1:n.79+1505_79+1508delinsTCAC ENSP00000497560.1:p.=
ENST00000311322.8:c.1018+1505_1018+1508delinsTCAC ENSP00000309757.6:p.=
NM_000237.2:c.1018+1505_1018+1508delinsTCAC NP_000228.1:p.=
NM_000237.3:c.1018+1505_1018+1508delinsTCAC MANE Select NP_000228.1:p.=