Canonical Allele Identifier: CA1769116509
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966771C= , CM000670.2:g.19966771C= GRCh38
NC_000008.10:g.19824282C= , CM000670.1:g.19824282C= GRCh37
NC_000008.9:g.19868562C= NCBI36
NG_008855.1:g.32701C=
NG_008855.2:g.70055C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1461C= MANE Select ENSP00000497642.1:n.*1461C=
ENST00000650478.1:c.1829C= ENSP00000497560.1:n.1829C=
ENST00000311322.8:c.*1461C= ENSP00000309757.6:n.*1461C=
NM_000237.2:c.*1461C= NP_000228.1:n.*1461C=
NM_000237.3:c.*1461C= MANE Select NP_000228.1:n.*1461C=