Canonical Allele Identifier: CA1769097893
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951893C= , CM000670.2:g.19951893C= GRCh38
NC_000008.10:g.19809404C= , CM000670.1:g.19809404C= GRCh37
NC_000008.9:g.19853684C= NCBI36
NG_008855.1:g.17823C=
NG_008855.2:g.55177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.374C= MANE Select ENSP00000497642.1:p.Ala125=
ENST00000311322.8:c.374C= ENSP00000309757.6:p.Ala125=
ENST00000520959.5:c.146C= ENSP00000428496.1:p.Ala49=
ENST00000524029.5:c.374C= ENSP00000428237.1:p.Ala125=
NM_000237.2:c.374C= NP_000228.1:p.Ala125=
NM_000237.3:c.374C= MANE Select NP_000228.1:p.Ala125=