Canonical Allele Identifier: CA580502352
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1214976921
gnomAD v2: 8-19813193-A-AT
gnomAD v3: 8-19955682-A-AT
gnomAD v4: 8-19955682-A-AT
MyVariant Identifiers: chr8:g.19813193_19813194insT (hg19) chr8:g.19955682_19955683insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955683dup , CM000670.2:g.19955683dup GRCh38
NC_000008.10:g.19813194dup , CM000670.1:g.19813194dup GRCh37
NC_000008.9:g.19857474dup NCBI36
NG_008855.1:g.21613dup
NG_008855.2:g.58967dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-158dup MANE Select ENSP00000497642.1:n.776-158dup
ENST00000311322.8:c.776-158dup ENSP00000309757.6:n.776-158dup
NM_000237.2:c.776-158dup NP_000228.1:n.776-158dup
NM_000237.3:c.776-158dup MANE Select NP_000228.1:n.776-158dup
Search 100 bp 5'
Search 100 bp 3'