Canonical Allele Identifier: CA1769083282
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939336_19939337delinsCT , CM000670.2:g.19939336_19939337delinsCT GRCh38
NC_000008.10:g.19796847_19796848delinsCT , CM000670.1:g.19796847_19796848delinsCT GRCh37
NC_000008.9:g.19841127_19841128delinsCT NCBI36
NG_008855.1:g.5266_5267delinsCT
NG_008855.2:g.42620_42621delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-105_-104delinsCT MANE Select ENSP00000497642.1:n.-105_-104delinsCT
ENST00000311322.8:c.-105_-104delinsCT ENSP00000309757.6:n.-105_-104delinsCT
ENST00000519773.1:c.-105_-104delinsCT ENSP00000431028.1:n.-105_-104delinsCT
ENST00000520959.5:c.-140-8844_-140-8843delinsCT ENSP00000428496.1:n.-140-8844_-140-8843delinsCT
ENST00000521994.1:n.81_82delinsCT
ENST00000522701.5:c.-105_-104delinsCT ENSP00000428557.1:n.-105_-104delinsCT
ENST00000524029.5:c.-105_-104delinsCT ENSP00000428237.1:n.-105_-104delinsCT
NM_000237.2:c.-105_-104delinsCT NP_000228.1:n.-105_-104delinsCT
NM_000237.3:c.-105_-104delinsCT MANE Select NP_000228.1:n.-105_-104delinsCT