Canonical Allele Identifier: CA1111553380
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590145835
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958032A>G , CM000670.2:g.19958032A>G GRCh38
NC_000008.10:g.19815543A>G , CM000670.1:g.19815543A>G GRCh37
NC_000008.9:g.19859823A>G NCBI36
NG_008855.1:g.23962A>G
NG_008855.2:g.61316A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1228A>G MANE Select ENSP00000497642.1:n.1019-1228A>G
ENST00000650478.1:c.79+1949A>G ENSP00000497560.1:n.79+1949A>G
ENST00000311322.8:c.1019-1228A>G ENSP00000309757.6:n.1019-1228A>G
NM_000237.2:c.1019-1228A>G NP_000228.1:n.1019-1228A>G
NM_000237.3:c.1019-1228A>G MANE Select NP_000228.1:n.1019-1228A>G
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