Canonical Allele Identifier: CA1769104466
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955848C= , CM000670.2:g.19955848C= GRCh38
NC_000008.10:g.19813359C= , CM000670.1:g.19813359C= GRCh37
NC_000008.9:g.19857639C= NCBI36
NG_008855.1:g.21778C=
NG_008855.2:g.59132C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.783C= MANE Select ENSP00000497642.1:p.Asp261=
ENST00000311322.8:c.783C= ENSP00000309757.6:p.Asp261=
NM_000237.2:c.783C= NP_000228.1:p.Asp261=
NM_000237.3:c.783C= MANE Select NP_000228.1:p.Asp261=