Canonical Allele Identifier: CA2779304517
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967045G>T , CM000670.2:g.19967045G>T GRCh38
NC_000008.10:g.19824556G>T , CM000670.1:g.19824556G>T GRCh37
NC_000008.9:g.19868836G>T NCBI36
NG_008855.1:g.32975G>T
NG_008855.2:g.70329G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1735G>T MANE Select ENSP00000497642.1:n.*1735G>T
ENST00000650478.1:c.2103G>T ENSP00000497560.1:n.2103G>T
ENST00000311322.8:c.*1735G>T ENSP00000309757.6:n.*1735G>T
NM_000237.2:c.*1735G>T NP_000228.1:n.*1735G>T
NM_000237.3:c.*1735G>T MANE Select NP_000228.1:n.*1735G>T