Canonical Allele Identifier: CA370467687
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951904A>G , CM000670.2:g.19951904A>G GRCh38
NC_000008.10:g.19809415A>G , CM000670.1:g.19809415A>G GRCh37
NC_000008.9:g.19853695A>G NCBI36
NG_008855.1:g.17834A>G
NG_008855.2:g.55188A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.385A>G MANE Select ENSP00000497642.1:p.Lys129Glu
ENST00000311322.8:c.385A>G ENSP00000309757.6:p.Lys129Glu
ENST00000520959.5:c.157A>G ENSP00000428496.1:p.Lys53Glu
ENST00000524029.5:c.385A>G ENSP00000428237.1:p.Lys129Glu
NM_000237.2:c.385A>G NP_000228.1:p.Lys129Glu
NM_000237.3:c.385A>G MANE Select NP_000228.1:p.Lys129Glu