Canonical Allele Identifier: CA1769116566
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966817G= , CM000670.2:g.19966817G= GRCh38
NC_000008.10:g.19824328G= , CM000670.1:g.19824328G= GRCh37
NC_000008.9:g.19868608G= NCBI36
NG_008855.1:g.32747G=
NG_008855.2:g.70101G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1507G= MANE Select ENSP00000497642.1:n.*1507G=
ENST00000650478.1:c.1875G= ENSP00000497560.1:n.1875G=
ENST00000311322.8:c.*1507G= ENSP00000309757.6:n.*1507G=
NM_000237.2:c.*1507G= NP_000228.1:n.*1507G=
NM_000237.3:c.*1507G= MANE Select NP_000228.1:n.*1507G=