Canonical Allele Identifier: CA1769116423
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590151766
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966704A>G , CM000670.2:g.19966704A>G GRCh38
NC_000008.10:g.19824215A>G , CM000670.1:g.19824215A>G GRCh37
NC_000008.9:g.19868495A>G NCBI36
NG_008855.1:g.32634A>G
NG_008855.2:g.69988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1394A>G MANE Select ENSP00000497642.1:n.*1394A>G
ENST00000650478.1:c.1762A>G ENSP00000497560.1:n.1762A>G
ENST00000311322.8:c.*1394A>G ENSP00000309757.6:n.*1394A>G
NM_000237.2:c.*1394A>G NP_000228.1:n.*1394A>G
NM_000237.3:c.*1394A>G MANE Select NP_000228.1:n.*1394A>G
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