Canonical Allele Identifier: CA2580596393
Gene: LPL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967052T>A , CM000670.2:g.19967052T>A GRCh38
NC_000008.10:g.19824563T>A , CM000670.1:g.19824563T>A GRCh37
NC_000008.9:g.19868843T>A NCBI36
NG_008855.1:g.32982T>A
NG_008855.2:g.70336T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1742T>A MANE Select ENSP00000497642.1:n.*1742T>A
ENST00000650478.1:c.2110T>A ENSP00000497560.1:n.2110T>A
ENST00000311322.8:c.*1742T>A ENSP00000309757.6:n.*1742T>A
NM_000237.2:c.*1742T>A NP_000228.1:n.*1742T>A
NM_000237.3:c.*1742T>A MANE Select NP_000228.1:n.*1742T>A
Search 100 bp 5'
Search 100 bp 3'