Canonical Allele Identifier: CA413172478

Gene: IQSEC2

Linked Data

• gnomAD v4: X-53256055-C-A
• MyVariant Identifiers: chrX:g.53285237C>A (hg19) ; chrX:g.53256055C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53256055C>A , CM000685.2:g.53256055C>A	GRCh38
NC_000023.10:g.53285237C>A , CM000685.1:g.53285237C>A	GRCh37
NC_000023.9:g.53301962C>A	NCBI36
NG_021296.1:g.70286G>T
NG_021296.2:g.70296G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.903G>T	ENSP00000516672.1:p.Glu301Asp
ENST00000638630.1:c.33G>T	ENSP00000492390.1:p.Glu11Asp
ENST00000640694.1:c.744G>T	ENSP00000492403.1:p.Glu248Asp
ENST00000642864.1:c.744G>T MANE Select	ENSP00000495726.1:p.Glu248Asp
ENST00000674510.1:c.744G>T	ENSP00000502054.1:p.Glu248Asp
ENST00000675719.1:c.714G>T	ENSP00000501927.1:p.Glu238Asp
ENST00000375365.2:c.129G>T	ENSP00000364514.2:p.Glu43Asp
ENST00000396435.7:c.744G>T	ENSP00000379712.3:p.Glu248Asp
NM_001111125.2:c.744G>T	NP_001104595.1:p.Glu248Asp
NM_015075.1:c.129G>T	NP_055890.1:p.Glu43Asp
XM_006724579.2:c.840G>T	XP_006724642.1:p.Glu280Asp
XM_006724580.2:c.129G>T	XP_006724643.1:p.Glu43Asp
XM_006724581.2:c.840G>T	XP_006724644.1:p.Glu280Asp
XM_006724582.2:c.840G>T	XP_006724645.1:p.Glu280Asp
XM_006724583.2:c.840G>T	XP_006724646.1:p.Glu280Asp
XM_006724584.2:c.840G>T	XP_006724647.1:p.Glu280Asp
XM_011530772.1:c.66G>T	XP_011529074.1:p.Glu22Asp
XM_011530773.1:c.33G>T	XP_011529075.1:p.Glu11Asp
XM_011530774.1:c.840G>T	XP_011529076.1:p.Glu280Asp
XM_011530775.1:c.840G>T	XP_011529077.1:p.Glu280Asp
XM_011530776.1:c.840G>T	XP_011529078.1:p.Glu280Asp
XM_011530777.1:c.840G>T	XP_011529079.1:p.Glu280Asp
XR_938365.1:n.1067G>T
XM_006724579.3:c.840G>T	XP_006724642.1:p.Glu280Asp
XM_006724580.3:c.129G>T	XP_006724643.1:p.Glu43Asp
XM_006724581.4:c.840G>T	XP_006724644.1:p.Glu280Asp
XM_006724582.4:c.840G>T	XP_006724645.1:p.Glu280Asp
XM_006724583.4:c.840G>T	XP_006724646.1:p.Glu280Asp
XM_006724584.3:c.840G>T	XP_006724647.1:p.Glu280Asp
XM_011530773.2:c.33G>T	XP_011529075.1:p.Glu11Asp
XM_011530774.3:c.840G>T	XP_011529076.1:p.Glu280Asp
XM_011530776.2:c.840G>T	XP_011529078.1:p.Glu280Asp
XM_011530777.2:c.840G>T	XP_011529079.1:p.Glu280Asp
XM_017029359.2:c.714G>T	XP_016884848.1:p.Glu238Asp
XM_017029360.1:c.246G>T	XP_016884849.1:p.Glu82Asp
XR_938365.2:n.1061G>T
NM_001111125.3:c.744G>T MANE Select	NP_001104595.1:p.Glu248Asp
NM_015075.2:c.129G>T	NP_055890.1:p.Glu43Asp