Canonical Allele Identifier: CA1769097427
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951755_19951758delinsGTCA , CM000670.2:g.19951755_19951758delinsGTCA GRCh38
NC_000008.10:g.19809266_19809269delinsGTCA , CM000670.1:g.19809266_19809269delinsGTCA GRCh37
NC_000008.9:g.19853546_19853549delinsGTCA NCBI36
NG_008855.1:g.17685_17688delinsGTCA
NG_008855.2:g.55039_55042delinsGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-14_250-11delinsGTCA MANE Select ENSP00000497642.1:n.250-14_250-11delinsGTCA
ENST00000311322.8:c.250-14_250-11delinsGTCA ENSP00000309757.6:n.250-14_250-11delinsGTCA
ENST00000520959.5:c.22-14_22-11delinsGTCA ENSP00000428496.1:n.22-14_22-11delinsGTCA
ENST00000521994.1:n.493_496delinsGTCA
ENST00000522701.5:c.250-14_250-11delinsGTCA ENSP00000428557.1:n.250-14_250-11delinsGTCA
ENST00000524029.5:c.250-14_250-11delinsGTCA ENSP00000428237.1:n.250-14_250-11delinsGTCA
NM_000237.2:c.250-14_250-11delinsGTCA NP_000228.1:n.250-14_250-11delinsGTCA
NM_000237.3:c.250-14_250-11delinsGTCA MANE Select NP_000228.1:n.250-14_250-11delinsGTCA