Canonical Allele Identifier: CA1769102017
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954176C= , CM000670.2:g.19954176C= GRCh38
NC_000008.10:g.19811687C= , CM000670.1:g.19811687C= GRCh37
NC_000008.9:g.19855967C= NCBI36
NG_008855.1:g.20106C=
NG_008855.2:g.57460C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.598C= MANE Select ENSP00000497642.1:p.Pro200=
ENST00000311322.8:c.598C= ENSP00000309757.6:p.Pro200=
NM_000237.2:c.598C= NP_000228.1:p.Pro200=
NM_000237.3:c.598C= MANE Select NP_000228.1:p.Pro200=