Canonical Allele Identifier: CA413163929

Gene: IQSEC2

Linked Data

• ClinVar Variation Id: 836419
• ClinVar RCV Id: RCV001037543 ; RCV002400222
• dbSNP Id: rs2074375518
• gnomAD v4: X-53250822-C-T
• MyVariant Identifiers: chrX:g.53280004C>T (hg19) ; chrX:g.53250822C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250822C>T , CM000685.2:g.53250822C>T	GRCh38
NC_000023.10:g.53280004C>T , CM000685.1:g.53280004C>T	GRCh37
NC_000023.9:g.53296729C>T	NCBI36
NG_021296.1:g.75519G>A
NG_021296.2:g.75529G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1913G>A	ENSP00000516672.1:p.Arg638Gln
ENST00000640694.1:c.1754G>A	ENSP00000492403.1:p.Arg585Gln
ENST00000642864.1:c.1754G>A MANE Select	ENSP00000495726.1:p.Arg585Gln
ENST00000674510.1:c.1754G>A	ENSP00000502054.1:p.Arg585Gln
ENST00000675719.1:c.1724G>A	ENSP00000501927.1:p.Arg575Gln
ENST00000375365.2:c.1139G>A	ENSP00000364514.2:p.Arg380Gln
ENST00000396435.7:c.1754G>A	ENSP00000379712.3:p.Arg585Gln
NM_001111125.2:c.1754G>A	NP_001104595.1:p.Arg585Gln
NM_015075.1:c.1139G>A	NP_055890.1:p.Arg380Gln
XM_006724579.2:c.1850G>A	XP_006724642.1:p.Arg617Gln
XM_006724580.2:c.1139G>A	XP_006724643.1:p.Arg380Gln
XM_006724581.2:c.1850G>A	XP_006724644.1:p.Arg617Gln
XM_006724582.2:c.1850G>A	XP_006724645.1:p.Arg617Gln
XM_006724583.2:c.1850G>A	XP_006724646.1:p.Arg617Gln
XM_006724584.2:c.1850G>A	XP_006724647.1:p.Arg617Gln
XM_011530772.1:c.1076G>A	XP_011529074.1:p.Arg359Gln
XM_011530773.1:c.1043G>A	XP_011529075.1:p.Arg348Gln
XM_011530774.1:c.1850G>A	XP_011529076.1:p.Arg617Gln
XM_011530775.1:c.1850G>A	XP_011529077.1:p.Arg617Gln
XM_011530776.1:c.1850G>A	XP_011529078.1:p.Arg617Gln
XM_011530777.1:c.1850G>A	XP_011529079.1:p.Arg617Gln
XR_938365.1:n.2077G>A
XM_006724579.3:c.1850G>A	XP_006724642.1:p.Arg617Gln
XM_006724580.3:c.1139G>A	XP_006724643.1:p.Arg380Gln
XM_006724581.4:c.1850G>A	XP_006724644.1:p.Arg617Gln
XM_006724582.4:c.1850G>A	XP_006724645.1:p.Arg617Gln
XM_006724583.4:c.1850G>A	XP_006724646.1:p.Arg617Gln
XM_006724584.3:c.1850G>A	XP_006724647.1:p.Arg617Gln
XM_011530773.2:c.1043G>A	XP_011529075.1:p.Arg348Gln
XM_011530774.3:c.1850G>A	XP_011529076.1:p.Arg617Gln
XM_011530776.2:c.1850G>A	XP_011529078.1:p.Arg617Gln
XM_011530777.2:c.1850G>A	XP_011529079.1:p.Arg617Gln
XM_017029359.2:c.1724G>A	XP_016884848.1:p.Arg575Gln
XM_017029360.1:c.1256G>A	XP_016884849.1:p.Arg419Gln
XR_938365.2:n.2071G>A
NM_001111125.3:c.1754G>A MANE Select	NP_001104595.1:p.Arg585Gln
NM_015075.2:c.1139G>A	NP_055890.1:p.Arg380Gln