Canonical Allele Identifier: CA1769104642
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955937G= , CM000670.2:g.19955937G= GRCh38
NC_000008.10:g.19813448G= , CM000670.1:g.19813448G= GRCh37
NC_000008.9:g.19857728G= NCBI36
NG_008855.1:g.21867G=
NG_008855.2:g.59221G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.872G= MANE Select ENSP00000497642.1:p.Cys291=
ENST00000311322.8:c.872G= ENSP00000309757.6:p.Cys291=
NM_000237.2:c.872G= NP_000228.1:p.Cys291=
NM_000237.3:c.872G= MANE Select NP_000228.1:p.Cys291=