Canonical Allele Identifier: CA1769110635
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960907A= , CM000670.2:g.19960907A= GRCh38
NC_000008.10:g.19818418A= , CM000670.1:g.19818418A= GRCh37
NC_000008.9:g.19862698A= NCBI36
NG_008855.1:g.26837A=
NG_008855.2:g.64191A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1146A= MANE Select ENSP00000497642.1:p.Glu382=
ENST00000650478.1:c.86A= ENSP00000497560.1:p.Lys29=
ENST00000311322.8:c.1146A= ENSP00000309757.6:p.Glu382=
NM_000237.2:c.1146A= NP_000228.1:p.Glu382=
NM_000237.3:c.1146A= MANE Select NP_000228.1:p.Glu382=