Canonical Allele Identifier: CA1769116360
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966645G= , CM000670.2:g.19966645G= GRCh38
NC_000008.10:g.19824156G= , CM000670.1:g.19824156G= GRCh37
NC_000008.9:g.19868436G= NCBI36
NG_008855.1:g.32575G=
NG_008855.2:g.69929G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1335G= MANE Select ENSP00000497642.1:n.*1335G=
ENST00000650478.1:c.1703G= ENSP00000497560.1:n.1703G=
ENST00000311322.8:c.*1335G= ENSP00000309757.6:n.*1335G=
NM_000237.2:c.*1335G= NP_000228.1:n.*1335G=
NM_000237.3:c.*1335G= MANE Select NP_000228.1:n.*1335G=