Canonical Allele Identifier: CA1769097926
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951915A= , CM000670.2:g.19951915A= GRCh38
NC_000008.10:g.19809426A= , CM000670.1:g.19809426A= GRCh37
NC_000008.9:g.19853706A= NCBI36
NG_008855.1:g.17845A=
NG_008855.2:g.55199A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.396A= MANE Select ENSP00000497642.1:p.Gly132=
ENST00000311322.8:c.396A= ENSP00000309757.6:p.Gly132=
ENST00000520959.5:c.168A= ENSP00000428496.1:p.Gly56=
NM_000237.2:c.396A= NP_000228.1:p.Gly132=
NM_000237.3:c.396A= MANE Select NP_000228.1:p.Gly132=