Canonical Allele Identifier: CA459719145
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 1604842
ClinVar RCV Id: RCV002159890
dbSNP Id: rs2128839569
gnomAD v4: 8-19960916-A-T
MyVariant Identifiers: chr8:g.19818427A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960916A>T , CM000670.2:g.19960916A>T GRCh38
NC_000008.10:g.19818427A>T , CM000670.1:g.19818427A>T GRCh37
NC_000008.9:g.19862707A>T NCBI36
NG_008855.1:g.26846A>T
NG_008855.2:g.64200A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1155A>T MANE Select ENSP00000497642.1:p.Thr385=
ENST00000650478.1:c.95A>T ENSP00000497560.1:p.Gln32Leu
ENST00000311322.8:c.1155A>T ENSP00000309757.6:p.Thr385=
NM_000237.2:c.1155A>T NP_000228.1:p.Thr385=
NM_000237.3:c.1155A>T MANE Select NP_000228.1:p.Thr385=
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