Canonical Allele Identifier: CA2779304250
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960785T>A , CM000670.2:g.19960785T>A GRCh38
NC_000008.10:g.19818296T>A , CM000670.1:g.19818296T>A GRCh37
NC_000008.9:g.19862576T>A NCBI36
NG_008855.1:g.26715T>A
NG_008855.2:g.64069T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-116T>A MANE Select ENSP00000497642.1:n.1140-116T>A
ENST00000650478.1:c.80-116T>A ENSP00000497560.1:n.80-116T>A
ENST00000311322.8:c.1140-116T>A ENSP00000309757.6:n.1140-116T>A
NM_000237.2:c.1140-116T>A NP_000228.1:n.1140-116T>A
NM_000237.3:c.1140-116T>A MANE Select NP_000228.1:n.1140-116T>A