Canonical Allele Identifier: CA2779304211
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952053T>G , CM000670.2:g.19952053T>G GRCh38
NC_000008.10:g.19809564T>G , CM000670.1:g.19809564T>G GRCh37
NC_000008.9:g.19853844T>G NCBI36
NG_008855.1:g.17983T>G
NG_008855.2:g.55337T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+105T>G MANE Select ENSP00000497642.1:n.429+105T>G
ENST00000311322.8:c.429+105T>G ENSP00000309757.6:n.429+105T>G
ENST00000520959.5:c.201+105T>G ENSP00000428496.1:n.201+105T>G
NM_000237.2:c.429+105T>G NP_000228.1:n.429+105T>G
NM_000237.3:c.429+105T>G MANE Select NP_000228.1:n.429+105T>G