Canonical Allele Identifier: CA516428067

Gene: IQSEC2

Linked Data

• dbSNP Id: rs782108139
• gnomAD v4: X-53248033-CAG-C
• MyVariant Identifiers: chrX:g.53277216_53277217del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248037_53248038del , CM000685.2:g.53248037_53248038del	GRCh38
NC_000023.10:g.53277219_53277220del , CM000685.1:g.53277219_53277220del	GRCh37
NC_000023.9:g.53293944_53293945del	NCBI36
NG_021296.1:g.78306_78307del
NG_021296.2:g.78316_78317del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.2741+79_2741+80del	ENSP00000516672.1:n.2741+79_2741+80del
ENST00000638521.1:c.534+79_534+80del
ENST00000638869.1:c.43+79_43+80del
ENST00000640694.1:c.2582+79_2582+80del	ENSP00000492403.1:n.2582+79_2582+80del
ENST00000642864.1:c.2582+79_2582+80del MANE Select	ENSP00000495726.1:n.2582+79_2582+80del
ENST00000674510.1:c.2582+79_2582+80del	ENSP00000502054.1:n.2582+79_2582+80del
ENST00000674761.1:n.333+79_333+80del
ENST00000675719.1:c.2552+79_2552+80del	ENSP00000501927.1:n.2552+79_2552+80del
ENST00000375365.2:c.1967+79_1967+80del	ENSP00000364514.2:n.1967+79_1967+80del
ENST00000396435.7:c.2582+79_2582+80del	ENSP00000379712.3:n.2582+79_2582+80del
NM_001111125.2:c.2582+79_2582+80del	NP_001104595.1:n.2582+79_2582+80del
NM_015075.1:c.1967+79_1967+80del	NP_055890.1:n.1967+79_1967+80del
XM_006724579.2:c.2678+79_2678+80del	XP_006724642.1:n.2678+79_2678+80del
XM_006724580.2:c.1967+79_1967+80del	XP_006724643.1:n.1967+79_1967+80del
XM_006724581.2:c.2678+79_2678+80del	XP_006724644.1:n.2678+79_2678+80del
XM_006724582.2:c.2678+79_2678+80del	XP_006724645.1:n.2678+79_2678+80del
XM_006724583.2:c.2678+79_2678+80del	XP_006724646.1:n.2678+79_2678+80del
XM_006724584.2:c.2678+79_2678+80del	XP_006724647.1:n.2678+79_2678+80del
XM_011530772.1:c.1904+79_1904+80del	XP_011529074.1:n.1904+79_1904+80del
XM_011530773.1:c.1871+79_1871+80del	XP_011529075.1:n.1871+79_1871+80del
XM_011530774.1:c.2678+79_2678+80del	XP_011529076.1:n.2678+79_2678+80del
XM_011530775.1:c.2678+79_2678+80del	XP_011529077.1:n.2678+79_2678+80del
XM_011530776.1:c.2678+79_2678+80del	XP_011529078.1:n.2678+79_2678+80del
XM_011530777.1:c.2678+79_2678+80del	XP_011529079.1:n.2678+79_2678+80del
XR_938365.1:n.2905+79_2905+80del
XM_006724579.3:c.2678+79_2678+80del	XP_006724642.1:n.2678+79_2678+80del
XM_006724580.3:c.1967+79_1967+80del	XP_006724643.1:n.1967+79_1967+80del
XM_006724581.4:c.2678+79_2678+80del	XP_006724644.1:n.2678+79_2678+80del
XM_006724582.4:c.2678+79_2678+80del	XP_006724645.1:n.2678+79_2678+80del
XM_006724583.4:c.2678+79_2678+80del	XP_006724646.1:n.2678+79_2678+80del
XM_006724584.3:c.2678+79_2678+80del	XP_006724647.1:n.2678+79_2678+80del
XM_011530773.2:c.1871+79_1871+80del	XP_011529075.1:n.1871+79_1871+80del
XM_011530774.3:c.2678+79_2678+80del	XP_011529076.1:n.2678+79_2678+80del
XM_011530776.2:c.2678+79_2678+80del	XP_011529078.1:n.2678+79_2678+80del
XM_011530777.2:c.2678+79_2678+80del	XP_011529079.1:n.2678+79_2678+80del
XM_017029359.2:c.2552+79_2552+80del	XP_016884848.1:n.2552+79_2552+80del
XM_017029360.1:c.2084+79_2084+80del	XP_016884849.1:n.2084+79_2084+80del
XR_938365.2:n.2899+79_2899+80del
NM_001111125.3:c.2582+79_2582+80del MANE Select	NP_001104595.1:n.2582+79_2582+80del
NM_015075.2:c.1967+79_1967+80del	NP_055890.1:n.1967+79_1967+80del