Canonical Allele Identifier: CA516428096

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53277319C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248137C>G , CM000685.2:g.53248137C>G	GRCh38
NC_000023.10:g.53277319C>G , CM000685.1:g.53277319C>G	GRCh37
NC_000023.9:g.53294044C>G	NCBI36
NG_021296.1:g.78204G>C
NG_021296.2:g.78214G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2718G>C	ENSP00000516672.1:p.Val906=
ENST00000638521.1:c.511G>C
ENST00000638869.1:c.20G>C
ENST00000640694.1:c.2559G>C	ENSP00000492403.1:p.Val853=
ENST00000642864.1:c.2559G>C MANE Select	ENSP00000495726.1:p.Val853=
ENST00000674510.1:c.2559G>C	ENSP00000502054.1:p.Val853=
ENST00000674761.1:n.310G>C
ENST00000675719.1:c.2529G>C	ENSP00000501927.1:p.Val843=
ENST00000375365.2:c.1944G>C	ENSP00000364514.2:p.Val648=
ENST00000396435.7:c.2559G>C	ENSP00000379712.3:p.Val853=
NM_001111125.2:c.2559G>C	NP_001104595.1:p.Val853=
NM_015075.1:c.1944G>C	NP_055890.1:p.Val648=
XM_006724579.2:c.2655G>C	XP_006724642.1:p.Val885=
XM_006724580.2:c.1944G>C	XP_006724643.1:p.Val648=
XM_006724581.2:c.2655G>C	XP_006724644.1:p.Val885=
XM_006724582.2:c.2655G>C	XP_006724645.1:p.Val885=
XM_006724583.2:c.2655G>C	XP_006724646.1:p.Val885=
XM_006724584.2:c.2655G>C	XP_006724647.1:p.Val885=
XM_011530772.1:c.1881G>C	XP_011529074.1:p.Val627=
XM_011530773.1:c.1848G>C	XP_011529075.1:p.Val616=
XM_011530774.1:c.2655G>C	XP_011529076.1:p.Val885=
XM_011530775.1:c.2655G>C	XP_011529077.1:p.Val885=
XM_011530776.1:c.2655G>C	XP_011529078.1:p.Val885=
XM_011530777.1:c.2655G>C	XP_011529079.1:p.Val885=
XR_938365.1:n.2882G>C
XM_006724579.3:c.2655G>C	XP_006724642.1:p.Val885=
XM_006724580.3:c.1944G>C	XP_006724643.1:p.Val648=
XM_006724581.4:c.2655G>C	XP_006724644.1:p.Val885=
XM_006724582.4:c.2655G>C	XP_006724645.1:p.Val885=
XM_006724583.4:c.2655G>C	XP_006724646.1:p.Val885=
XM_006724584.3:c.2655G>C	XP_006724647.1:p.Val885=
XM_011530773.2:c.1848G>C	XP_011529075.1:p.Val616=
XM_011530774.3:c.2655G>C	XP_011529076.1:p.Val885=
XM_011530776.2:c.2655G>C	XP_011529078.1:p.Val885=
XM_011530777.2:c.2655G>C	XP_011529079.1:p.Val885=
XM_017029359.2:c.2529G>C	XP_016884848.1:p.Val843=
XM_017029360.1:c.2061G>C	XP_016884849.1:p.Val687=
XR_938365.2:n.2876G>C
NM_001111125.3:c.2559G>C MANE Select	NP_001104595.1:p.Val853=
NM_015075.2:c.1944G>C	NP_055890.1:p.Val648=