Canonical Allele Identifier: CA1769110699
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960949G= , CM000670.2:g.19960949G= GRCh38
NC_000008.10:g.19818460G= , CM000670.1:g.19818460G= GRCh37
NC_000008.9:g.19862740G= NCBI36
NG_008855.1:g.26879G=
NG_008855.2:g.64233G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1188G= MANE Select ENSP00000497642.1:p.Glu396=
ENST00000650478.1:c.128G= ENSP00000497560.1:n.128G=
ENST00000311322.8:c.1188G= ENSP00000309757.6:p.Glu396=
NM_000237.2:c.1188G= NP_000228.1:p.Glu396=
NM_000237.3:c.1188G= MANE Select NP_000228.1:p.Glu396=