Canonical Allele Identifier: CA1769106654
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957588T= , CM000670.2:g.19957588T= GRCh38
NC_000008.10:g.19815099T= , CM000670.1:g.19815099T= GRCh37
NC_000008.9:g.19859379T= NCBI36
NG_008855.1:g.23518T=
NG_008855.2:g.60872T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1505T= MANE Select ENSP00000497642.1:n.1018+1505T=
ENST00000650478.1:c.79+1505T= ENSP00000497560.1:n.79+1505T=
ENST00000311322.8:c.1018+1505T= ENSP00000309757.6:n.1018+1505T=
NM_000237.2:c.1018+1505T= NP_000228.1:n.1018+1505T=
NM_000237.3:c.1018+1505T= MANE Select NP_000228.1:n.1018+1505T=