Canonical Allele Identifier: CA1769097669
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951832G= , CM000670.2:g.19951832G= GRCh38
NC_000008.10:g.19809343G= , CM000670.1:g.19809343G= GRCh37
NC_000008.9:g.19853623G= NCBI36
NG_008855.1:g.17762G=
NG_008855.2:g.55116G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.313G= MANE Select ENSP00000497642.1:p.Asp105=
ENST00000311322.8:c.313G= ENSP00000309757.6:p.Asp105=
ENST00000520959.5:c.85G= ENSP00000428496.1:p.Asp29=
ENST00000522701.5:c.313G= ENSP00000428557.1:p.Asp105=
ENST00000524029.5:c.313G= ENSP00000428237.1:p.Asp105=
NM_000237.2:c.313G= NP_000228.1:p.Asp105=
NM_000237.3:c.313G= MANE Select NP_000228.1:p.Asp105=