Canonical Allele Identifier: CA580158137
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs10634207
gnomAD v2: 8-19815499-TTTTATTTA-T
gnomAD v3: 8-19957988-TTTTATTTA-T
gnomAD v4: 8-19957988-TTTTATTTA-T
MyVariant Identifiers: chr8:g.19815508_19815515del (hg19) chr8:g.19815500_19815507del (hg19) chr8:g.19957997_19958004del (hg38) chr8:g.19957989_19957996del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958028_19958035del , CM000670.2:g.19958028_19958035del GRCh38
NC_000008.10:g.19815539_19815546del , CM000670.1:g.19815539_19815546del GRCh37
NC_000008.9:g.19859819_19859826del NCBI36
NG_008855.1:g.23958_23965del
NG_008855.2:g.61312_61319del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1232_1019-1225del MANE Select ENSP00000497642.1:n.1019-1232_1019-1225del
ENST00000650478.1:c.79+1945_79+1952del ENSP00000497560.1:n.79+1945_79+1952del
ENST00000311322.8:c.1019-1232_1019-1225del ENSP00000309757.6:n.1019-1232_1019-1225del
NM_000237.2:c.1019-1232_1019-1225del NP_000228.1:n.1019-1232_1019-1225del
NM_000237.3:c.1019-1232_1019-1225del MANE Select NP_000228.1:n.1019-1232_1019-1225del
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