Canonical Allele Identifier: CA2502622109
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966694_19966695insA , CM000670.2:g.19966694_19966695insA GRCh38
NC_000008.10:g.19824205_19824206insA , CM000670.1:g.19824205_19824206insA GRCh37
NC_000008.9:g.19868485_19868486insA NCBI36
NG_008855.1:g.32624_32625insA
NG_008855.2:g.69978_69979insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1384_*1385insA MANE Select ENSP00000497642.1:n.*1384_*1385insA
ENST00000650478.1:c.1752_1753insA ENSP00000497560.1:n.1752_1753insA
ENST00000311322.8:c.*1384_*1385insA ENSP00000309757.6:n.*1384_*1385insA
NM_000237.2:c.*1384_*1385insA NP_000228.1:n.*1384_*1385insA
NM_000237.3:c.*1384_*1385insA MANE Select NP_000228.1:n.*1384_*1385insA