Canonical Allele Identifier: CA413156978

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53277336C>G (hg19) ; chrX:g.53248154C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248154C>G , CM000685.2:g.53248154C>G	GRCh38
NC_000023.10:g.53277336C>G , CM000685.1:g.53277336C>G	GRCh37
NC_000023.9:g.53294061C>G	NCBI36
NG_021296.1:g.78187G>C
NG_021296.2:g.78197G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2701G>C	ENSP00000516672.1:p.Gly901Arg
ENST00000638521.1:c.494G>C
ENST00000638869.1:c.3G>C
ENST00000640694.1:c.2542G>C	ENSP00000492403.1:p.Gly848Arg
ENST00000642864.1:c.2542G>C MANE Select	ENSP00000495726.1:p.Gly848Arg
ENST00000674510.1:c.2542G>C	ENSP00000502054.1:p.Gly848Arg
ENST00000674761.1:n.293G>C
ENST00000675719.1:c.2512G>C	ENSP00000501927.1:p.Gly838Arg
ENST00000375365.2:c.1927G>C	ENSP00000364514.2:p.Gly643Arg
ENST00000396435.7:c.2542G>C	ENSP00000379712.3:p.Gly848Arg
NM_001111125.2:c.2542G>C	NP_001104595.1:p.Gly848Arg
NM_015075.1:c.1927G>C	NP_055890.1:p.Gly643Arg
XM_006724579.2:c.2638G>C	XP_006724642.1:p.Gly880Arg
XM_006724580.2:c.1927G>C	XP_006724643.1:p.Gly643Arg
XM_006724581.2:c.2638G>C	XP_006724644.1:p.Gly880Arg
XM_006724582.2:c.2638G>C	XP_006724645.1:p.Gly880Arg
XM_006724583.2:c.2638G>C	XP_006724646.1:p.Gly880Arg
XM_006724584.2:c.2638G>C	XP_006724647.1:p.Gly880Arg
XM_011530772.1:c.1864G>C	XP_011529074.1:p.Gly622Arg
XM_011530773.1:c.1831G>C	XP_011529075.1:p.Gly611Arg
XM_011530774.1:c.2638G>C	XP_011529076.1:p.Gly880Arg
XM_011530775.1:c.2638G>C	XP_011529077.1:p.Gly880Arg
XM_011530776.1:c.2638G>C	XP_011529078.1:p.Gly880Arg
XM_011530777.1:c.2638G>C	XP_011529079.1:p.Gly880Arg
XR_938365.1:n.2865G>C
XM_006724579.3:c.2638G>C	XP_006724642.1:p.Gly880Arg
XM_006724580.3:c.1927G>C	XP_006724643.1:p.Gly643Arg
XM_006724581.4:c.2638G>C	XP_006724644.1:p.Gly880Arg
XM_006724582.4:c.2638G>C	XP_006724645.1:p.Gly880Arg
XM_006724583.4:c.2638G>C	XP_006724646.1:p.Gly880Arg
XM_006724584.3:c.2638G>C	XP_006724647.1:p.Gly880Arg
XM_011530773.2:c.1831G>C	XP_011529075.1:p.Gly611Arg
XM_011530774.3:c.2638G>C	XP_011529076.1:p.Gly880Arg
XM_011530776.2:c.2638G>C	XP_011529078.1:p.Gly880Arg
XM_011530777.2:c.2638G>C	XP_011529079.1:p.Gly880Arg
XM_017029359.2:c.2512G>C	XP_016884848.1:p.Gly838Arg
XM_017029360.1:c.2044G>C	XP_016884849.1:p.Gly682Arg
XR_938365.2:n.2859G>C
NM_001111125.3:c.2542G>C MANE Select	NP_001104595.1:p.Gly848Arg
NM_015075.2:c.1927G>C	NP_055890.1:p.Gly643Arg