Canonical Allele Identifier: CA1769083314
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590134147
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939351A>C , CM000670.2:g.19939351A>C GRCh38
NC_000008.10:g.19796862A>C , CM000670.1:g.19796862A>C GRCh37
NC_000008.9:g.19841142A>C NCBI36
NG_008855.1:g.5281A>C
NG_008855.2:g.42635A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-90A>C MANE Select ENSP00000497642.1:n.-90A>C
ENST00000311322.8:c.-90A>C ENSP00000309757.6:n.-90A>C
ENST00000519773.1:c.-90A>C ENSP00000431028.1:n.-90A>C
ENST00000520959.5:c.-140-8829A>C ENSP00000428496.1:n.-140-8829A>C
ENST00000521994.1:n.96A>C
ENST00000522701.5:c.-90A>C ENSP00000428557.1:n.-90A>C
ENST00000524029.5:c.-90A>C ENSP00000428237.1:n.-90A>C
NM_000237.2:c.-90A>C NP_000228.1:n.-90A>C
NM_000237.3:c.-90A>C MANE Select NP_000228.1:n.-90A>C
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