Canonical Allele Identifier: CA2779304298
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961707A>G , CM000670.2:g.19961707A>G GRCh38
NC_000008.10:g.19819218A>G , CM000670.1:g.19819218A>G GRCh37
NC_000008.9:g.19863498A>G NCBI36
NG_008855.1:g.27637A>G
NG_008855.2:g.64991A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1323-408A>G MANE Select ENSP00000497642.1:n.1323-408A>G
ENST00000650478.1:c.263-408A>G ENSP00000497560.1:n.263-408A>G
ENST00000311322.8:c.1323-408A>G ENSP00000309757.6:n.1323-408A>G
NM_000237.2:c.1323-408A>G NP_000228.1:n.1323-408A>G
NM_000237.3:c.1323-408A>G MANE Select NP_000228.1:n.1323-408A>G
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