Canonical Allele Identifier: CA1769096892
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951471A= , CM000670.2:g.19951471A= GRCh38
NC_000008.10:g.19808982A= , CM000670.1:g.19808982A= GRCh37
NC_000008.9:g.19853262A= NCBI36
NG_008855.1:g.17401A=
NG_008855.2:g.54755A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-298A= MANE Select ENSP00000497642.1:n.250-298A=
ENST00000311322.8:c.250-298A= ENSP00000309757.6:n.250-298A=
ENST00000520959.5:c.22-298A= ENSP00000428496.1:n.22-298A=
ENST00000521994.1:n.435-226A=
ENST00000522701.5:c.250-298A= ENSP00000428557.1:n.250-298A=
ENST00000524029.5:c.250-298A= ENSP00000428237.1:n.250-298A=
NM_000237.2:c.250-298A= NP_000228.1:n.250-298A=
NM_000237.3:c.250-298A= MANE Select NP_000228.1:n.250-298A=
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