Canonical Allele Identifier: CA370467499
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951821A>G , CM000670.2:g.19951821A>G GRCh38
NC_000008.10:g.19809332A>G , CM000670.1:g.19809332A>G GRCh37
NC_000008.9:g.19853612A>G NCBI36
NG_008855.1:g.17751A>G
NG_008855.2:g.55105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.302A>G MANE Select ENSP00000497642.1:p.Lys101Arg
ENST00000311322.8:c.302A>G ENSP00000309757.6:p.Lys101Arg
ENST00000520959.5:c.74A>G ENSP00000428496.1:p.Lys25Arg
ENST00000521994.1:n.559A>G
ENST00000522701.5:c.302A>G ENSP00000428557.1:p.Lys101Arg
ENST00000524029.5:c.302A>G ENSP00000428237.1:p.Lys101Arg
NM_000237.2:c.302A>G NP_000228.1:p.Lys101Arg
NM_000237.3:c.302A>G MANE Select NP_000228.1:p.Lys101Arg