Canonical Allele Identifier: CA1769103148
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954525A= , CM000670.2:g.19954525A= GRCh38
NC_000008.10:g.19812036A= , CM000670.1:g.19812036A= GRCh37
NC_000008.9:g.19856316A= NCBI36
NG_008855.1:g.20455A=
NG_008855.2:g.57809A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+172A= MANE Select ENSP00000497642.1:n.775+172A=
ENST00000311322.8:c.775+172A= ENSP00000309757.6:n.775+172A=
NM_000237.2:c.775+172A= NP_000228.1:n.775+172A=
NM_000237.3:c.775+172A= MANE Select NP_000228.1:n.775+172A=