Canonical Allele Identifier: CA370464607
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1396954757

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939451A>G , CM000670.2:g.19939451A>G GRCh38
NC_000008.10:g.19796962A>G , CM000670.1:g.19796962A>G GRCh37
NC_000008.9:g.19841242A>G NCBI36
NG_008855.1:g.5381A>G
NG_008855.2:g.42735A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.11A>G MANE Select ENSP00000497642.1:p.Lys4Arg
ENST00000311322.8:c.11A>G ENSP00000309757.6:p.Lys4Arg
ENST00000519773.1:c.11A>G ENSP00000431028.1:p.Lys4Arg
ENST00000520959.5:c.-140-8729A>G ENSP00000428496.1:n.-140-8729A>G
ENST00000521994.1:n.196A>G
ENST00000522701.5:c.11A>G ENSP00000428557.1:p.Lys4Arg
ENST00000523696.1:n.80A>G
ENST00000524029.5:c.11A>G ENSP00000428237.1:p.Lys4Arg
NM_000237.2:c.11A>G NP_000228.1:p.Lys4Arg
NM_000237.3:c.11A>G MANE Select NP_000228.1:p.Lys4Arg