Canonical Allele Identifier: CA2511371184
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957382C>A , CM000670.2:g.19957382C>A GRCh38
NC_000008.10:g.19814893C>A , CM000670.1:g.19814893C>A GRCh37
NC_000008.9:g.19859173C>A NCBI36
NG_008855.1:g.23312C>A
NG_008855.2:g.60666C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1018+1299C>A MANE Select ENSP00000497642.1:n.1018+1299C>A
ENST00000650478.1:c.79+1299C>A ENSP00000497560.1:n.79+1299C>A
ENST00000311322.8:c.1018+1299C>A ENSP00000309757.6:n.1018+1299C>A
NM_000237.2:c.1018+1299C>A NP_000228.1:n.1018+1299C>A
NM_000237.3:c.1018+1299C>A MANE Select NP_000228.1:n.1018+1299C>A