Canonical Allele Identifier: CA2779304168
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951589_19951590dup , CM000670.2:g.19951589_19951590dup GRCh38
NC_000008.10:g.19809100_19809101dup , CM000670.1:g.19809100_19809101dup GRCh37
NC_000008.9:g.19853380_19853381dup NCBI36
NG_008855.1:g.17519_17520dup
NG_008855.2:g.54873_54874dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-180_250-179dup MANE Select ENSP00000497642.1:n.250-180_250-179dup
ENST00000311322.8:c.250-180_250-179dup ENSP00000309757.6:n.250-180_250-179dup
ENST00000520959.5:c.22-180_22-179dup ENSP00000428496.1:n.22-180_22-179dup
ENST00000521994.1:n.435-108_435-107dup
ENST00000522701.5:c.250-180_250-179dup ENSP00000428557.1:n.250-180_250-179dup
ENST00000524029.5:c.250-180_250-179dup ENSP00000428237.1:n.250-180_250-179dup
NM_000237.2:c.250-180_250-179dup NP_000228.1:n.250-180_250-179dup
NM_000237.3:c.250-180_250-179dup MANE Select NP_000228.1:n.250-180_250-179dup