Canonical Allele Identifier: CA1769116489
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966757G= , CM000670.2:g.19966757G= GRCh38
NC_000008.10:g.19824268G= , CM000670.1:g.19824268G= GRCh37
NC_000008.9:g.19868548G= NCBI36
NG_008855.1:g.32687G=
NG_008855.2:g.70041G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1447G= MANE Select ENSP00000497642.1:n.*1447G=
ENST00000650478.1:c.1815G= ENSP00000497560.1:n.1815G=
ENST00000311322.8:c.*1447G= ENSP00000309757.6:n.*1447G=
NM_000237.2:c.*1447G= NP_000228.1:n.*1447G=
NM_000237.3:c.*1447G= MANE Select NP_000228.1:n.*1447G=
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