Canonical Allele Identifier: CA1769098107
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069938885
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951991T>A , CM000670.2:g.19951991T>A GRCh38
NC_000008.10:g.19809502T>A , CM000670.1:g.19809502T>A GRCh37
NC_000008.9:g.19853782T>A NCBI36
NG_008855.1:g.17921T>A
NG_008855.2:g.55275T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+43T>A MANE Select ENSP00000497642.1:n.429+43T>A
ENST00000311322.8:c.429+43T>A ENSP00000309757.6:n.429+43T>A
ENST00000520959.5:c.201+43T>A ENSP00000428496.1:n.201+43T>A
NM_000237.2:c.429+43T>A NP_000228.1:n.429+43T>A
NM_000237.3:c.429+43T>A MANE Select NP_000228.1:n.429+43T>A
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