Canonical Allele Identifier: CA1769097707
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951844A= , CM000670.2:g.19951844A= GRCh38
NC_000008.10:g.19809355A= , CM000670.1:g.19809355A= GRCh37
NC_000008.9:g.19853635A= NCBI36
NG_008855.1:g.17774A=
NG_008855.2:g.55128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.325A= MANE Select ENSP00000497642.1:p.Ile109=
ENST00000311322.8:c.325A= ENSP00000309757.6:p.Ile109=
ENST00000520959.5:c.97A= ENSP00000428496.1:p.Ile33=
ENST00000524029.5:c.325A= ENSP00000428237.1:p.Ile109=
NM_000237.2:c.325A= NP_000228.1:p.Ile109=
NM_000237.3:c.325A= MANE Select NP_000228.1:p.Ile109=