Canonical Allele Identifier: CA1769101923
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954146G= , CM000670.2:g.19954146G= GRCh38
NC_000008.10:g.19811657G= , CM000670.1:g.19811657G= GRCh37
NC_000008.9:g.19855937G= NCBI36
NG_008855.1:g.20076G=
NG_008855.2:g.57430G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.568G= MANE Select ENSP00000497642.1:p.Glu190=
ENST00000311322.8:c.568G= ENSP00000309757.6:p.Glu190=
ENST00000520959.5:c.340G= ENSP00000428496.1:p.Glu114=
NM_000237.2:c.568G= NP_000228.1:p.Glu190=
NM_000237.3:c.568G= MANE Select NP_000228.1:p.Glu190=