Canonical Allele Identifier: CA173374801
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19948173T>G , CM000670.2:g.19948173T>G GRCh38
NC_000008.10:g.19805684T>G , CM000670.1:g.19805684T>G GRCh37
NC_000008.9:g.19849964T>G NCBI36
NG_008855.1:g.14103T>G
NG_008855.2:g.51457T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.89-7T>G MANE Select ENSP00000497642.1:n.89-7T>G
ENST00000311322.8:c.89-7T>G ENSP00000309757.6:n.89-7T>G
ENST00000519773.1:c.*126-7T>G ENSP00000431028.1:n.*126-7T>G
ENST00000520959.5:c.-140-7T>G ENSP00000428496.1:n.-140-7T>G
ENST00000521994.1:n.274-7T>G
ENST00000522701.5:c.89-7T>G ENSP00000428557.1:n.89-7T>G
ENST00000523696.1:n.158-7T>G
ENST00000524029.5:c.89-7T>G ENSP00000428237.1:n.89-7T>G
NM_000237.2:c.89-7T>G NP_000228.1:n.89-7T>G
NM_000237.3:c.89-7T>G MANE Select NP_000228.1:n.89-7T>G