Canonical Allele Identifier: CA1111569202
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590134135
gnomAD v3: 8-19939343-A-G
gnomAD v4: 8-19939343-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939343A>G , CM000670.2:g.19939343A>G GRCh38
NC_000008.10:g.19796854A>G , CM000670.1:g.19796854A>G GRCh37
NC_000008.9:g.19841134A>G NCBI36
NG_008855.1:g.5273A>G
NG_008855.2:g.42627A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-98A>G MANE Select ENSP00000497642.1:n.-98A>G
ENST00000311322.8:c.-98A>G ENSP00000309757.6:n.-98A>G
ENST00000519773.1:c.-98A>G ENSP00000431028.1:n.-98A>G
ENST00000520959.5:c.-140-8837A>G ENSP00000428496.1:n.-140-8837A>G
ENST00000521994.1:n.88A>G
ENST00000522701.5:c.-98A>G ENSP00000428557.1:n.-98A>G
ENST00000524029.5:c.-98A>G ENSP00000428237.1:n.-98A>G
NM_000237.2:c.-98A>G NP_000228.1:n.-98A>G
NM_000237.3:c.-98A>G MANE Select NP_000228.1:n.-98A>G
Search 100 bp 5'
Search 100 bp 3'