Canonical Allele Identifier: CA1769103200
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954565_19954568delinsGAGC , CM000670.2:g.19954565_19954568delinsGAGC GRCh38
NC_000008.10:g.19812076_19812079delinsGAGC , CM000670.1:g.19812076_19812079delinsGAGC GRCh37
NC_000008.9:g.19856356_19856359delinsGAGC NCBI36
NG_008855.1:g.20495_20498delinsGAGC
NG_008855.2:g.57849_57852delinsGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+212_775+215delinsGAGC MANE Select ENSP00000497642.1:n.775+212_775+215delinsGAGC
ENST00000311322.8:c.775+212_775+215delinsGAGC ENSP00000309757.6:n.775+212_775+215delinsGAGC
NM_000237.2:c.775+212_775+215delinsGAGC NP_000228.1:n.775+212_775+215delinsGAGC
NM_000237.3:c.775+212_775+215delinsGAGC MANE Select NP_000228.1:n.775+212_775+215delinsGAGC