Canonical Allele Identifier: CA4655519
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs762691925
ExAC: 8:19811899 CT / C
gnomAD v2: 8-19811899-CT-C
gnomAD v4: 8-19954388-CT-C
MyVariant Identifiers: chr8:g.19811900del (hg19) chr8:g.19954389del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954390del , CM000670.2:g.19954390del GRCh38
NC_000008.10:g.19811901del , CM000670.1:g.19811901del GRCh37
NC_000008.9:g.19856181del NCBI36
NG_008855.1:g.20320del
NG_008855.2:g.57674del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+37del MANE Select ENSP00000497642.1:n.775+37del
ENST00000311322.8:c.775+37del ENSP00000309757.6:n.775+37del
NM_000237.2:c.775+37del NP_000228.1:n.775+37del
NM_000237.3:c.775+37del MANE Select NP_000228.1:n.775+37del
Search 100 bp 5'
Search 100 bp 3'