Canonical Allele Identifier: CA1769098169
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952046T= , CM000670.2:g.19952046T= GRCh38
NC_000008.10:g.19809557T= , CM000670.1:g.19809557T= GRCh37
NC_000008.9:g.19853837T= NCBI36
NG_008855.1:g.17976T=
NG_008855.2:g.55330T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+98T= MANE Select ENSP00000497642.1:n.429+98T=
ENST00000311322.8:c.429+98T= ENSP00000309757.6:n.429+98T=
ENST00000520959.5:c.201+98T= ENSP00000428496.1:n.201+98T=
NM_000237.2:c.429+98T= NP_000228.1:n.429+98T=
NM_000237.3:c.429+98T= MANE Select NP_000228.1:n.429+98T=