Canonical Allele Identifier: CA1769097573
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951810C= , CM000670.2:g.19951810C= GRCh38
NC_000008.10:g.19809321C= , CM000670.1:g.19809321C= GRCh37
NC_000008.9:g.19853601C= NCBI36
NG_008855.1:g.17740C=
NG_008855.2:g.55094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.291C= MANE Select ENSP00000497642.1:p.Ala97=
ENST00000311322.8:c.291C= ENSP00000309757.6:p.Ala97=
ENST00000520959.5:c.63C= ENSP00000428496.1:p.Ala21=
ENST00000521994.1:n.548C=
ENST00000522701.5:c.291C= ENSP00000428557.1:p.Ala97=
ENST00000524029.5:c.291C= ENSP00000428237.1:p.Ala97=
NM_000237.2:c.291C= NP_000228.1:p.Ala97=
NM_000237.3:c.291C= MANE Select NP_000228.1:p.Ala97=