Canonical Allele Identifier: CA1769097647
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951828A= , CM000670.2:g.19951828A= GRCh38
NC_000008.10:g.19809339A= , CM000670.1:g.19809339A= GRCh37
NC_000008.9:g.19853619A= NCBI36
NG_008855.1:g.17758A=
NG_008855.2:g.55112A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.309A= MANE Select ENSP00000497642.1:p.Glu103=
ENST00000311322.8:c.309A= ENSP00000309757.6:p.Glu103=
ENST00000520959.5:c.81A= ENSP00000428496.1:p.Glu27=
ENST00000521994.1:n.566A=
ENST00000522701.5:c.309A= ENSP00000428557.1:p.Glu103=
ENST00000524029.5:c.309A= ENSP00000428237.1:p.Glu103=
NM_000237.2:c.309A= NP_000228.1:p.Glu103=
NM_000237.3:c.309A= MANE Select NP_000228.1:p.Glu103=