Canonical Allele Identifier: CA2839228408
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962917T>A , CM000670.2:g.19962917T>A GRCh38
NC_000008.10:g.19820428T>A , CM000670.1:g.19820428T>A GRCh37
NC_000008.9:g.19864708T>A NCBI36
NG_008855.1:g.28847T>A
NG_008855.2:g.66201T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1427+698T>A MANE Select ENSP00000497642.1:n.1427+698T>A
ENST00000650478.1:c.367+698T>A ENSP00000497560.1:n.367+698T>A
ENST00000311322.8:c.1427+698T>A ENSP00000309757.6:n.1427+698T>A
NM_000237.2:c.1427+698T>A NP_000228.1:n.1427+698T>A
NM_000237.3:c.1427+698T>A MANE Select NP_000228.1:n.1427+698T>A