Canonical Allele Identifier: CA1769104437
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955821_19955823delinsGGT , CM000670.2:g.19955821_19955823delinsGGT GRCh38
NC_000008.10:g.19813332_19813334delinsGGT , CM000670.1:g.19813332_19813334delinsGGT GRCh37
NC_000008.9:g.19857612_19857614delinsGGT NCBI36
NG_008855.1:g.21751_21753delinsGGT
NG_008855.2:g.59105_59107delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-20_776-18delinsGGT MANE Select ENSP00000497642.1:n.776-20_776-18delinsGGT
ENST00000311322.8:c.776-20_776-18delinsGGT ENSP00000309757.6:n.776-20_776-18delinsGGT
NM_000237.2:c.776-20_776-18delinsGGT NP_000228.1:n.776-20_776-18delinsGGT
NM_000237.3:c.776-20_776-18delinsGGT MANE Select NP_000228.1:n.776-20_776-18delinsGGT