Canonical Allele Identifier: CA370467519
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951826G>A , CM000670.2:g.19951826G>A GRCh38
NC_000008.10:g.19809337G>A , CM000670.1:g.19809337G>A GRCh37
NC_000008.9:g.19853617G>A NCBI36
NG_008855.1:g.17756G>A
NG_008855.2:g.55110G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.307G>A MANE Select ENSP00000497642.1:p.Glu103Lys
ENST00000311322.8:c.307G>A ENSP00000309757.6:p.Glu103Lys
ENST00000520959.5:c.79G>A ENSP00000428496.1:p.Glu27Lys
ENST00000521994.1:n.564G>A
ENST00000522701.5:c.307G>A ENSP00000428557.1:p.Glu103Lys
ENST00000524029.5:c.307G>A ENSP00000428237.1:p.Glu103Lys
NM_000237.2:c.307G>A NP_000228.1:p.Glu103Lys
NM_000237.3:c.307G>A MANE Select NP_000228.1:p.Glu103Lys