Canonical Allele Identifier: CA1769098435
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952164T= , CM000670.2:g.19952164T= GRCh38
NC_000008.10:g.19809675T= , CM000670.1:g.19809675T= GRCh37
NC_000008.9:g.19853955T= NCBI36
NG_008855.1:g.18094T=
NG_008855.2:g.55448T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+216T= MANE Select ENSP00000497642.1:n.429+216T=
ENST00000311322.8:c.429+216T= ENSP00000309757.6:n.429+216T=
ENST00000520959.5:c.201+216T= ENSP00000428496.1:n.201+216T=
NM_000237.2:c.429+216T= NP_000228.1:n.429+216T=
NM_000237.3:c.429+216T= MANE Select NP_000228.1:n.429+216T=
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