Canonical Allele Identifier: CA1769106718
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957649T= , CM000670.2:g.19957649T= GRCh38
NC_000008.10:g.19815160T= , CM000670.1:g.19815160T= GRCh37
NC_000008.9:g.19859440T= NCBI36
NG_008855.1:g.23579T=
NG_008855.2:g.60933T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1566T= MANE Select ENSP00000497642.1:n.1018+1566T=
ENST00000650478.1:c.79+1566T= ENSP00000497560.1:n.79+1566T=
ENST00000311322.8:c.1018+1566T= ENSP00000309757.6:n.1018+1566T=
NM_000237.2:c.1018+1566T= NP_000228.1:n.1018+1566T=
NM_000237.3:c.1018+1566T= MANE Select NP_000228.1:n.1018+1566T=