Canonical Allele Identifier: CA1769097995
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951948G= , CM000670.2:g.19951948G= GRCh38
NC_000008.10:g.19809459G= , CM000670.1:g.19809459G= GRCh37
NC_000008.9:g.19853739G= NCBI36
NG_008855.1:g.17878G=
NG_008855.2:g.55232G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429G= MANE Select ENSP00000497642.1:p.Glu143=
ENST00000311322.8:c.429G= ENSP00000309757.6:p.Glu143=
ENST00000520959.5:c.201G= ENSP00000428496.1:p.Glu67=
NM_000237.2:c.429G= NP_000228.1:p.Glu143=
NM_000237.3:c.429G= MANE Select NP_000228.1:p.Glu143=