Canonical Allele Identifier: CA1769106707
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957637_19957638delinsGT , CM000670.2:g.19957637_19957638delinsGT GRCh38
NC_000008.10:g.19815148_19815149delinsGT , CM000670.1:g.19815148_19815149delinsGT GRCh37
NC_000008.9:g.19859428_19859429delinsGT NCBI36
NG_008855.1:g.23567_23568delinsGT
NG_008855.2:g.60921_60922delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1554_1018+1555delinsGT MANE Select ENSP00000497642.1:n.1018+1554_1018+1555de...
ENST00000650478.1:c.79+1554_79+1555delinsGT ENSP00000497560.1:n.79+1554_79+1555delins...
ENST00000311322.8:c.1018+1554_1018+1555delinsGT ENSP00000309757.6:n.1018+1554_1018+1555de...
NM_000237.2:c.1018+1554_1018+1555delinsGT NP_000228.1:n.1018+1554_1018+1555delinsGT...
NM_000237.3:c.1018+1554_1018+1555delinsGT MANE Select NP_000228.1:n.1018+1554_1018+1555delinsGT...