Canonical Allele Identifier: CA1769102620
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954243G= , CM000670.2:g.19954243G= GRCh38
NC_000008.10:g.19811754G= , CM000670.1:g.19811754G= GRCh37
NC_000008.9:g.19856034G= NCBI36
NG_008855.1:g.20173G=
NG_008855.2:g.57527G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.665G= MANE Select ENSP00000497642.1:p.Gly222=
ENST00000311322.8:c.665G= ENSP00000309757.6:p.Gly222=
NM_000237.2:c.665G= NP_000228.1:p.Gly222=
NM_000237.3:c.665G= MANE Select NP_000228.1:p.Gly222=