Canonical Allele Identifier: CA658824141
Gene: IQSEC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 546336
ClinVar RCV Id: RCV000658197
dbSNP Id: rs1556862426

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53248105_53248120del , CM000685.2:g.53248105_53248120del GRCh38
NC_000023.10:g.53277287_53277302del , CM000685.1:g.53277287_53277302del GRCh37
NC_000023.9:g.53294012_53294027del NCBI36
NG_021296.1:g.78224_78239del
NG_021296.2:g.78234_78249del

Transcript Alleles

HGVS Amino-acid change
ENST00000706952.1:c.2738_2741+12del
ENST00000638521.1:c.531_534+12del
ENST00000638869.1:c.40_43+12del
ENST00000640694.1:c.2579_2582+12del
ENST00000642864.1:c.2579_2582+12del
ENST00000674510.1:c.2579_2582+12del
ENST00000674761.1:n.330_333+12del
ENST00000675719.1:c.2549_2552+12del
ENST00000375365.2:c.1964_1967+12del
ENST00000396435.7:c.2579_2582+12del
NM_001111125.2:c.2579_2582+12del
NM_015075.1:c.1964_1967+12del
XM_006724579.2:c.2675_2678+12del
XM_006724580.2:c.1964_1967+12del
XM_006724581.2:c.2675_2678+12del
XM_006724582.2:c.2675_2678+12del
XM_006724583.2:c.2675_2678+12del
XM_006724584.2:c.2675_2678+12del
XM_011530772.1:c.1901_1904+12del
XM_011530773.1:c.1868_1871+12del
XM_011530774.1:c.2675_2678+12del
XM_011530775.1:c.2675_2678+12del
XM_011530776.1:c.2675_2678+12del
XM_011530777.1:c.2675_2678+12del
XR_938365.1:n.2902_2905+12del
XM_006724579.3:c.2675_2678+12del
XM_006724580.3:c.1964_1967+12del
XM_006724581.4:c.2675_2678+12del
XM_006724582.4:c.2675_2678+12del
XM_006724583.4:c.2675_2678+12del
XM_006724584.3:c.2675_2678+12del
XM_011530773.2:c.1868_1871+12del
XM_011530774.3:c.2675_2678+12del
XM_011530776.2:c.2675_2678+12del
XM_011530777.2:c.2675_2678+12del
XM_017029359.2:c.2549_2552+12del
XM_017029360.1:c.2081_2084+12del
XR_938365.2:n.2896_2899+12del
NM_001111125.3:c.2579_2582+12del
NM_015075.2:c.1964_1967+12del