Canonical Allele Identifier: CA1769116900
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070096795
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967155T>A , CM000670.2:g.19967155T>A GRCh38
NC_000008.10:g.19824666T>A , CM000670.1:g.19824666T>A GRCh37
NC_000008.9:g.19868946T>A NCBI36
NG_008855.1:g.33085T>A
NG_008855.2:g.70439T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1845T>A MANE Select ENSP00000497642.1:n.*1845T>A
ENST00000650478.1:c.2213T>A ENSP00000497560.1:n.2213T>A
ENST00000311322.8:c.*1845T>A ENSP00000309757.6:n.*1845T>A
NM_000237.2:c.*1845T>A NP_000228.1:n.*1845T>A
NM_000237.3:c.*1845T>A MANE Select NP_000228.1:n.*1845T>A
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