Canonical Allele Identifier: CA2580803859
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957371G>T , CM000670.2:g.19957371G>T GRCh38
NC_000008.10:g.19814882G>T , CM000670.1:g.19814882G>T GRCh37
NC_000008.9:g.19859162G>T NCBI36
NG_008855.1:g.23301G>T
NG_008855.2:g.60655G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1018+1288G>T MANE Select ENSP00000497642.1:n.1018+1288G>T
ENST00000650478.1:c.79+1288G>T ENSP00000497560.1:n.79+1288G>T
ENST00000311322.8:c.1018+1288G>T ENSP00000309757.6:n.1018+1288G>T
NM_000237.2:c.1018+1288G>T NP_000228.1:n.1018+1288G>T
NM_000237.3:c.1018+1288G>T MANE Select NP_000228.1:n.1018+1288G>T