Canonical Allele Identifier: CA1769107026
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070001380
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957939del , CM000670.2:g.19957939del GRCh38
NC_000008.10:g.19815450del , CM000670.1:g.19815450del GRCh37
NC_000008.9:g.19859730del NCBI36
NG_008855.1:g.23869del
NG_008855.2:g.61223del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1321del MANE Select ENSP00000497642.1:n.1019-1321del
ENST00000650478.1:c.79+1856del ENSP00000497560.1:n.79+1856del
ENST00000311322.8:c.1019-1321del ENSP00000309757.6:n.1019-1321del
NM_000237.2:c.1019-1321del NP_000228.1:n.1019-1321del
NM_000237.3:c.1019-1321del MANE Select NP_000228.1:n.1019-1321del
Search 100 bp 5'
Search 100 bp 3'