Canonical Allele Identifier: CA1769102966
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954378A= , CM000670.2:g.19954378A= GRCh38
NC_000008.10:g.19811889A= , CM000670.1:g.19811889A= GRCh37
NC_000008.9:g.19856169A= NCBI36
NG_008855.1:g.20308A=
NG_008855.2:g.57662A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+25A= MANE Select ENSP00000497642.1:n.775+25A=
ENST00000311322.8:c.775+25A= ENSP00000309757.6:n.775+25A=
NM_000237.2:c.775+25A= NP_000228.1:n.775+25A=
NM_000237.3:c.775+25A= MANE Select NP_000228.1:n.775+25A=