Canonical Allele Identifier: CA849564673
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1200280110
gnomAD v3: 8-19961705-A-AC
gnomAD v4: 8-19961705-A-AC
MyVariant Identifiers: chr8:g.19819216_19819217insC (hg19) chr8:g.19961705_19961706insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961705_19961706insC , CM000670.2:g.19961705_19961706insC GRCh38
NC_000008.10:g.19819216_19819217insC , CM000670.1:g.19819216_19819217insC GRCh37
NC_000008.9:g.19863496_19863497insC NCBI36
NG_008855.1:g.27635_27636insC
NG_008855.2:g.64989_64990insC

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1323-410_1323-409insC MANE Select ENSP00000497642.1:n.1323-410_1323-409insC
ENST00000650478.1:c.263-410_263-409insC ENSP00000497560.1:n.263-410_263-409insC
ENST00000311322.8:c.1323-410_1323-409insC ENSP00000309757.6:n.1323-410_1323-409insC
NM_000237.2:c.1323-410_1323-409insC NP_000228.1:n.1323-410_1323-409insC
NM_000237.3:c.1323-410_1323-409insC MANE Select NP_000228.1:n.1323-410_1323-409insC
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