Canonical Allele Identifier: CA1769110758
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960993G= , CM000670.2:g.19960993G= GRCh38
NC_000008.10:g.19818504G= , CM000670.1:g.19818504G= GRCh37
NC_000008.9:g.19862784G= NCBI36
NG_008855.1:g.26923G=
NG_008855.2:g.64277G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1232G= MANE Select ENSP00000497642.1:p.Ser411=
ENST00000650478.1:c.172G= ENSP00000497560.1:n.172G=
ENST00000311322.8:c.1232G= ENSP00000309757.6:p.Ser411=
NM_000237.2:c.1232G= NP_000228.1:p.Ser411=
NM_000237.3:c.1232G= MANE Select NP_000228.1:p.Ser411=