Canonical Allele Identifier: CA1769103245
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954614A= , CM000670.2:g.19954614A= GRCh38
NC_000008.10:g.19812125A= , CM000670.1:g.19812125A= GRCh37
NC_000008.9:g.19856405A= NCBI36
NG_008855.1:g.20544A=
NG_008855.2:g.57898A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+261A= MANE Select ENSP00000497642.1:n.775+261A=
ENST00000311322.8:c.775+261A= ENSP00000309757.6:n.775+261A=
NM_000237.2:c.775+261A= NP_000228.1:n.775+261A=
NM_000237.3:c.775+261A= MANE Select NP_000228.1:n.775+261A=