Canonical Allele Identifier: CA1769102602
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954238C= , CM000670.2:g.19954238C= GRCh38
NC_000008.10:g.19811749C= , CM000670.1:g.19811749C= GRCh37
NC_000008.9:g.19856029C= NCBI36
NG_008855.1:g.20168C=
NG_008855.2:g.57522C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.660C= MANE Select ENSP00000497642.1:p.Ser220=
ENST00000311322.8:c.660C= ENSP00000309757.6:p.Ser220=
NM_000237.2:c.660C= NP_000228.1:p.Ser220=
NM_000237.3:c.660C= MANE Select NP_000228.1:p.Ser220=