Canonical Allele Identifier: CA1769104135
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955501_19955502delinsAG , CM000670.2:g.19955501_19955502delinsAG GRCh38
NC_000008.10:g.19813012_19813013delinsAG , CM000670.1:g.19813012_19813013delinsAG GRCh37
NC_000008.9:g.19857292_19857293delinsAG NCBI36
NG_008855.1:g.21431_21432delinsAG
NG_008855.2:g.58785_58786delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-340_776-339delinsAG MANE Select ENSP00000497642.1:n.776-340_776-339delinsAG
ENST00000311322.8:c.776-340_776-339delinsAG ENSP00000309757.6:n.776-340_776-339delinsAG
NM_000237.2:c.776-340_776-339delinsAG NP_000228.1:n.776-340_776-339delinsAG
NM_000237.3:c.776-340_776-339delinsAG MANE Select NP_000228.1:n.776-340_776-339delinsAG