Canonical Allele Identifier: CA619561920
Gene: IQGAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1230743421
gnomAD v2: 15-91044423-AAAAC-A
gnomAD v3: 15-90501191-AAAAC-A
gnomAD v4: 15-90501191-AAAAC-A
MyVariant Identifiers: chr15:g.91044424_91044427del (hg19) chr15:g.90501192_90501195del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90501195_90501198del , CM000677.2:g.90501195_90501198del GRCh38
NC_000015.9:g.91044427_91044430del , CM000677.1:g.91044427_91044430del GRCh37
NC_000015.8:g.88845431_88845434del NCBI36
NG_052946.1:g.117955_117958del

Transcript Alleles

HGVS Amino-acid change
ENST00000268182.10:c.*1087_*1090del MANE Select ENSP00000268182.5:n.*1087_*1090del
ENST00000268182.9:c.*1087_*1090del ENSP00000268182.5:n.*1087_*1090del
ENST00000558957.1:n.2119_2122del
ENST00000561086.1:n.1828_1831del
NM_003870.3:c.*1087_*1090del NP_003861.1:n.*1087_*1090del
XR_001751409.2:n.6190_6193del
NM_003870.4:c.*1087_*1090del MANE Select NP_003861.1:n.*1087_*1090del
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