Canonical Allele Identifier: CA370467536
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951833A>G , CM000670.2:g.19951833A>G GRCh38
NC_000008.10:g.19809344A>G , CM000670.1:g.19809344A>G GRCh37
NC_000008.9:g.19853624A>G NCBI36
NG_008855.1:g.17763A>G
NG_008855.2:g.55117A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.314A>G MANE Select ENSP00000497642.1:p.Asp105Gly
ENST00000311322.8:c.314A>G ENSP00000309757.6:p.Asp105Gly
ENST00000520959.5:c.86A>G ENSP00000428496.1:p.Asp29Gly
ENST00000522701.5:c.314A>G ENSP00000428557.1:p.Asp105Gly
ENST00000524029.5:c.314A>G ENSP00000428237.1:p.Asp105Gly
NM_000237.2:c.314A>G NP_000228.1:p.Asp105Gly
NM_000237.3:c.314A>G MANE Select NP_000228.1:p.Asp105Gly