Canonical Allele Identifier: CA10602403
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 226450
ClinVar RCV Id: RCV000258507
dbSNP Id: rs886037775
MyVariant Identifiers: chr8:g.19818459A>T (hg19) chr8:g.19960948A>T (hg38)
PubMed: PMID:28548960
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960948A>T , CM000670.2:g.19960948A>T GRCh38
NC_000008.10:g.19818459A>T , CM000670.1:g.19818459A>T GRCh37
NC_000008.9:g.19862739A>T NCBI36
NG_008855.1:g.26878A>T
NG_008855.2:g.64232A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1187A>T MANE Select ENSP00000497642.1:p.Glu396Val
ENST00000650478.1:c.127A>T ENSP00000497560.1:n.127A>T
ENST00000311322.8:c.1187A>T ENSP00000309757.6:p.Glu396Val
NM_000237.2:c.1187A>T NP_000228.1:p.Glu396Val
NM_000237.3:c.1187A>T MANE Select NP_000228.1:p.Glu396Val
Search 100 bp 5'
Search 100 bp 3'