Canonical Allele Identifier: CA1769104116
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955486C= , CM000670.2:g.19955486C= GRCh38
NC_000008.10:g.19812997C= , CM000670.1:g.19812997C= GRCh37
NC_000008.9:g.19857277C= NCBI36
NG_008855.1:g.21416C=
NG_008855.2:g.58770C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-355C= MANE Select ENSP00000497642.1:n.776-355C=
ENST00000311322.8:c.776-355C= ENSP00000309757.6:n.776-355C=
NM_000237.2:c.776-355C= NP_000228.1:n.776-355C=
NM_000237.3:c.776-355C= MANE Select NP_000228.1:n.776-355C=
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