Canonical Allele Identifier: CA1769101931
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954148G= , CM000670.2:g.19954148G= GRCh38
NC_000008.10:g.19811659G= , CM000670.1:g.19811659G= GRCh37
NC_000008.9:g.19855939G= NCBI36
NG_008855.1:g.20078G=
NG_008855.2:g.57432G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.570G= MANE Select ENSP00000497642.1:p.Glu190=
ENST00000311322.8:c.570G= ENSP00000309757.6:p.Glu190=
ENST00000520959.5:c.342G= ENSP00000428496.1:p.Glu114=
NM_000237.2:c.570G= NP_000228.1:p.Glu190=
NM_000237.3:c.570G= MANE Select NP_000228.1:p.Glu190=