Canonical Allele Identifier: CA1769097045
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1563572459
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951533G>A , CM000670.2:g.19951533G>A GRCh38
NC_000008.10:g.19809044G>A , CM000670.1:g.19809044G>A GRCh37
NC_000008.9:g.19853324G>A NCBI36
NG_008855.1:g.17463G>A
NG_008855.2:g.54817G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-236G>A MANE Select ENSP00000497642.1:n.250-236G>A
ENST00000311322.8:c.250-236G>A ENSP00000309757.6:n.250-236G>A
ENST00000520959.5:c.22-236G>A ENSP00000428496.1:n.22-236G>A
ENST00000521994.1:n.435-164G>A
ENST00000522701.5:c.250-236G>A ENSP00000428557.1:n.250-236G>A
ENST00000524029.5:c.250-236G>A ENSP00000428237.1:n.250-236G>A
NM_000237.2:c.250-236G>A NP_000228.1:n.250-236G>A
NM_000237.3:c.250-236G>A MANE Select NP_000228.1:n.250-236G>A
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