Canonical Allele Identifier: CA370638711
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960992A>G , CM000670.2:g.19960992A>G GRCh38
NC_000008.10:g.19818503A>G , CM000670.1:g.19818503A>G GRCh37
NC_000008.9:g.19862783A>G NCBI36
NG_008855.1:g.26922A>G
NG_008855.2:g.64276A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1231A>G MANE Select ENSP00000497642.1:p.Ser411Gly
ENST00000650478.1:c.171A>G ENSP00000497560.1:n.171A>G
ENST00000311322.8:c.1231A>G ENSP00000309757.6:p.Ser411Gly
NM_000237.2:c.1231A>G NP_000228.1:p.Ser411Gly
NM_000237.3:c.1231A>G MANE Select NP_000228.1:p.Ser411Gly