Canonical Allele Identifier: CA1769098239
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952085A= , CM000670.2:g.19952085A= GRCh38
NC_000008.10:g.19809596A= , CM000670.1:g.19809596A= GRCh37
NC_000008.9:g.19853876A= NCBI36
NG_008855.1:g.18015A=
NG_008855.2:g.55369A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+137A= MANE Select ENSP00000497642.1:n.429+137A=
ENST00000311322.8:c.429+137A= ENSP00000309757.6:n.429+137A=
ENST00000520959.5:c.201+137A= ENSP00000428496.1:n.201+137A=
NM_000237.2:c.429+137A= NP_000228.1:n.429+137A=
NM_000237.3:c.429+137A= MANE Select NP_000228.1:n.429+137A=