Canonical Allele Identifier: CA413148965

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53270999C>G (hg19) ; chrX:g.53241817C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241817C>G , CM000685.2:g.53241817C>G	GRCh38
NC_000023.10:g.53270999C>G , CM000685.1:g.53270999C>G	GRCh37
NC_000023.9:g.53287724C>G	NCBI36
NG_021296.1:g.84524G>C
NG_021296.2:g.84534G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.3141G>C	ENSP00000516672.1:p.Gln1047His
ENST00000638521.1:c.934G>C
ENST00000638869.1:c.443G>C
ENST00000639642.1:c.272G>C
ENST00000640005.1:c.45G>C	ENSP00000491293.1:p.Gln15His
ENST00000640694.1:c.2982G>C	ENSP00000492403.1:p.Gln994His
ENST00000642864.1:c.2982G>C MANE Select	ENSP00000495726.1:p.Gln994His
ENST00000674510.1:c.2982G>C	ENSP00000502054.1:p.Gln994His
ENST00000674761.1:n.1289G>C
ENST00000675719.1:c.2952G>C	ENSP00000501927.1:p.Gln984His
ENST00000375365.2:c.2367G>C	ENSP00000364514.2:p.Gln789His
ENST00000396435.7:c.2982G>C	ENSP00000379712.3:p.Gln994His
NM_001111125.2:c.2982G>C	NP_001104595.1:p.Gln994His
NM_015075.1:c.2367G>C	NP_055890.1:p.Gln789His
XM_006724579.2:c.3078G>C	XP_006724642.1:p.Gln1026His
XM_006724580.2:c.2367G>C	XP_006724643.1:p.Gln789His
XM_006724581.2:c.3078G>C	XP_006724644.1:p.Gln1026His
XM_006724582.2:c.3078G>C	XP_006724645.1:p.Gln1026His
XM_006724583.2:c.3078G>C	XP_006724646.1:p.Gln1026His
XM_006724584.2:c.3078G>C	XP_006724647.1:p.Gln1026His
XM_011530772.1:c.2304G>C	XP_011529074.1:p.Gln768His
XM_011530773.1:c.2271G>C	XP_011529075.1:p.Gln757His
XM_011530774.1:c.3078G>C	XP_011529076.1:p.Gln1026His
XM_011530775.1:c.3078G>C	XP_011529077.1:p.Gln1026His
XM_011530776.1:c.3078G>C	XP_011529078.1:p.Gln1026His
XM_011530777.1:c.3078G>C	XP_011529079.1:p.Gln1026His
XR_938365.1:n.3305G>C
XM_006724579.3:c.3078G>C	XP_006724642.1:p.Gln1026His
XM_006724580.3:c.2367G>C	XP_006724643.1:p.Gln789His
XM_006724581.4:c.3078G>C	XP_006724644.1:p.Gln1026His
XM_006724582.4:c.3078G>C	XP_006724645.1:p.Gln1026His
XM_006724583.4:c.3078G>C	XP_006724646.1:p.Gln1026His
XM_006724584.3:c.3078G>C	XP_006724647.1:p.Gln1026His
XM_011530773.2:c.2271G>C	XP_011529075.1:p.Gln757His
XM_011530774.3:c.3078G>C	XP_011529076.1:p.Gln1026His
XM_011530776.2:c.3078G>C	XP_011529078.1:p.Gln1026His
XM_011530777.2:c.3078G>C	XP_011529079.1:p.Gln1026His
XM_017029359.2:c.2952G>C	XP_016884848.1:p.Gln984His
XM_017029360.1:c.2484G>C	XP_016884849.1:p.Gln828His
XR_938365.2:n.3299G>C
NM_001111125.3:c.2982G>C MANE Select	NP_001104595.1:p.Gln994His
NM_015075.2:c.2367G>C	NP_055890.1:p.Gln789His