Canonical Allele Identifier: CA1769104644
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955938C= , CM000670.2:g.19955938C= GRCh38
NC_000008.10:g.19813449C= , CM000670.1:g.19813449C= GRCh37
NC_000008.9:g.19857729C= NCBI36
NG_008855.1:g.21868C=
NG_008855.2:g.59222C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.873C= MANE Select ENSP00000497642.1:p.Cys291=
ENST00000311322.8:c.873C= ENSP00000309757.6:p.Cys291=
NM_000237.2:c.873C= NP_000228.1:p.Cys291=
NM_000237.3:c.873C= MANE Select NP_000228.1:p.Cys291=