Canonical Allele Identifier: CA1769106501
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957479_19957481delinsTAA , CM000670.2:g.19957479_19957481delinsTAA GRCh38
NC_000008.10:g.19814990_19814992delinsTAA , CM000670.1:g.19814990_19814992delinsTAA GRCh37
NC_000008.9:g.19859270_19859272delinsTAA NCBI36
NG_008855.1:g.23409_23411delinsTAA
NG_008855.2:g.60763_60765delinsTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1396_1018+1398delinsTAA MANE Select ENSP00000497642.1:n.1018+1396_1018+1398de...
ENST00000650478.1:c.79+1396_79+1398delinsTAA ENSP00000497560.1:n.79+1396_79+1398delins...
ENST00000311322.8:c.1018+1396_1018+1398delinsTAA ENSP00000309757.6:n.1018+1396_1018+1398de...
NM_000237.2:c.1018+1396_1018+1398delinsTAA NP_000228.1:n.1018+1396_1018+1398delinsTA...
NM_000237.3:c.1018+1396_1018+1398delinsTAA MANE Select NP_000228.1:n.1018+1396_1018+1398delinsTA...