Canonical Allele Identifier: CA1111574293
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069934370
gnomAD v3: 8-19951567-A-G
gnomAD v4: 8-19951567-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951567A>G , CM000670.2:g.19951567A>G GRCh38
NC_000008.10:g.19809078A>G , CM000670.1:g.19809078A>G GRCh37
NC_000008.9:g.19853358A>G NCBI36
NG_008855.1:g.17497A>G
NG_008855.2:g.54851A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-202A>G MANE Select ENSP00000497642.1:n.250-202A>G
ENST00000311322.8:c.250-202A>G ENSP00000309757.6:n.250-202A>G
ENST00000520959.5:c.22-202A>G ENSP00000428496.1:n.22-202A>G
ENST00000521994.1:n.435-130A>G
ENST00000522701.5:c.250-202A>G ENSP00000428557.1:n.250-202A>G
ENST00000524029.5:c.250-202A>G ENSP00000428237.1:n.250-202A>G
NM_000237.2:c.250-202A>G NP_000228.1:n.250-202A>G
NM_000237.3:c.250-202A>G MANE Select NP_000228.1:n.250-202A>G
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