Canonical Allele Identifier: CA413172263

Gene: IQSEC2

Linked Data

• ClinVar Variation Id: 1357312
• ClinVar RCV Id: RCV001878293
• dbSNP Id: rs1556865162
• MyVariant Identifiers: chrX:g.53285203C>T (hg19) ; chrX:g.53256021C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53256021C>T , CM000685.2:g.53256021C>T	GRCh38
NC_000023.10:g.53285203C>T , CM000685.1:g.53285203C>T	GRCh37
NC_000023.9:g.53301928C>T	NCBI36
NG_021296.1:g.70320G>A
NG_021296.2:g.70330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.937G>A	ENSP00000516672.1:p.Val313Ile
ENST00000638630.1:c.67G>A	ENSP00000492390.1:p.Val23Ile
ENST00000640694.1:c.778G>A	ENSP00000492403.1:p.Val260Ile
ENST00000642864.1:c.778G>A MANE Select	ENSP00000495726.1:p.Val260Ile
ENST00000674510.1:c.778G>A	ENSP00000502054.1:p.Val260Ile
ENST00000675719.1:c.748G>A	ENSP00000501927.1:p.Val250Ile
ENST00000375365.2:c.163G>A	ENSP00000364514.2:p.Val55Ile
ENST00000396435.7:c.778G>A	ENSP00000379712.3:p.Val260Ile
NM_001111125.2:c.778G>A	NP_001104595.1:p.Val260Ile
NM_015075.1:c.163G>A	NP_055890.1:p.Val55Ile
XM_006724579.2:c.874G>A	XP_006724642.1:p.Val292Ile
XM_006724580.2:c.163G>A	XP_006724643.1:p.Val55Ile
XM_006724581.2:c.874G>A	XP_006724644.1:p.Val292Ile
XM_006724582.2:c.874G>A	XP_006724645.1:p.Val292Ile
XM_006724583.2:c.874G>A	XP_006724646.1:p.Val292Ile
XM_006724584.2:c.874G>A	XP_006724647.1:p.Val292Ile
XM_011530772.1:c.100G>A	XP_011529074.1:p.Val34Ile
XM_011530773.1:c.67G>A	XP_011529075.1:p.Val23Ile
XM_011530774.1:c.874G>A	XP_011529076.1:p.Val292Ile
XM_011530775.1:c.874G>A	XP_011529077.1:p.Val292Ile
XM_011530776.1:c.874G>A	XP_011529078.1:p.Val292Ile
XM_011530777.1:c.874G>A	XP_011529079.1:p.Val292Ile
XR_938365.1:n.1101G>A
XM_006724579.3:c.874G>A	XP_006724642.1:p.Val292Ile
XM_006724580.3:c.163G>A	XP_006724643.1:p.Val55Ile
XM_006724581.4:c.874G>A	XP_006724644.1:p.Val292Ile
XM_006724582.4:c.874G>A	XP_006724645.1:p.Val292Ile
XM_006724583.4:c.874G>A	XP_006724646.1:p.Val292Ile
XM_006724584.3:c.874G>A	XP_006724647.1:p.Val292Ile
XM_011530773.2:c.67G>A	XP_011529075.1:p.Val23Ile
XM_011530774.3:c.874G>A	XP_011529076.1:p.Val292Ile
XM_011530776.2:c.874G>A	XP_011529078.1:p.Val292Ile
XM_011530777.2:c.874G>A	XP_011529079.1:p.Val292Ile
XM_017029359.2:c.748G>A	XP_016884848.1:p.Val250Ile
XM_017029360.1:c.280G>A	XP_016884849.1:p.Val94Ile
XR_938365.2:n.1095G>A
NM_001111125.3:c.778G>A MANE Select	NP_001104595.1:p.Val260Ile
NM_015075.2:c.163G>A	NP_055890.1:p.Val55Ile