Canonical Allele Identifier: CA1111552228
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069976201
gnomAD v3: 8-19955537-TA-T
gnomAD v4: 8-19955537-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955540del , CM000670.2:g.19955540del GRCh38
NC_000008.10:g.19813051del , CM000670.1:g.19813051del GRCh37
NC_000008.9:g.19857331del NCBI36
NG_008855.1:g.21470del
NG_008855.2:g.58824del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-301del MANE Select ENSP00000497642.1:n.776-301del
ENST00000311322.8:c.776-301del ENSP00000309757.6:n.776-301del
NM_000237.2:c.776-301del NP_000228.1:n.776-301del
NM_000237.3:c.776-301del MANE Select NP_000228.1:n.776-301del
Search 100 bp 5'
Search 100 bp 3'