Canonical Allele Identifier: CA1769101852
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954125G= , CM000670.2:g.19954125G= GRCh38
NC_000008.10:g.19811636G= , CM000670.1:g.19811636G= GRCh37
NC_000008.9:g.19855916G= NCBI36
NG_008855.1:g.20055G=
NG_008855.2:g.57409G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.547G= MANE Select ENSP00000497642.1:p.Asp183=
ENST00000311322.8:c.547G= ENSP00000309757.6:p.Asp183=
ENST00000520959.5:c.319G= ENSP00000428496.1:p.Asp107=
NM_000237.2:c.547G= NP_000228.1:p.Asp183=
NM_000237.3:c.547G= MANE Select NP_000228.1:p.Asp183=