Canonical Allele Identifier: CA413156845

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53277308A>G (hg19) ; chrX:g.53248126A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248126A>G , CM000685.2:g.53248126A>G	GRCh38
NC_000023.10:g.53277308A>G , CM000685.1:g.53277308A>G	GRCh37
NC_000023.9:g.53294033A>G	NCBI36
NG_021296.1:g.78215T>C
NG_021296.2:g.78225T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.2729T>C	ENSP00000516672.1:p.Ile910Thr
ENST00000638521.1:c.522T>C
ENST00000638869.1:c.31T>C
ENST00000640694.1:c.2570T>C	ENSP00000492403.1:p.Ile857Thr
ENST00000642864.1:c.2570T>C MANE Select	ENSP00000495726.1:p.Ile857Thr
ENST00000674510.1:c.2570T>C	ENSP00000502054.1:p.Ile857Thr
ENST00000674761.1:n.321T>C
ENST00000675719.1:c.2540T>C	ENSP00000501927.1:p.Ile847Thr
ENST00000375365.2:c.1955T>C	ENSP00000364514.2:p.Ile652Thr
ENST00000396435.7:c.2570T>C	ENSP00000379712.3:p.Ile857Thr
NM_001111125.2:c.2570T>C	NP_001104595.1:p.Ile857Thr
NM_015075.1:c.1955T>C	NP_055890.1:p.Ile652Thr
XM_006724579.2:c.2666T>C	XP_006724642.1:p.Ile889Thr
XM_006724580.2:c.1955T>C	XP_006724643.1:p.Ile652Thr
XM_006724581.2:c.2666T>C	XP_006724644.1:p.Ile889Thr
XM_006724582.2:c.2666T>C	XP_006724645.1:p.Ile889Thr
XM_006724583.2:c.2666T>C	XP_006724646.1:p.Ile889Thr
XM_006724584.2:c.2666T>C	XP_006724647.1:p.Ile889Thr
XM_011530772.1:c.1892T>C	XP_011529074.1:p.Ile631Thr
XM_011530773.1:c.1859T>C	XP_011529075.1:p.Ile620Thr
XM_011530774.1:c.2666T>C	XP_011529076.1:p.Ile889Thr
XM_011530775.1:c.2666T>C	XP_011529077.1:p.Ile889Thr
XM_011530776.1:c.2666T>C	XP_011529078.1:p.Ile889Thr
XM_011530777.1:c.2666T>C	XP_011529079.1:p.Ile889Thr
XR_938365.1:n.2893T>C
XM_006724579.3:c.2666T>C	XP_006724642.1:p.Ile889Thr
XM_006724580.3:c.1955T>C	XP_006724643.1:p.Ile652Thr
XM_006724581.4:c.2666T>C	XP_006724644.1:p.Ile889Thr
XM_006724582.4:c.2666T>C	XP_006724645.1:p.Ile889Thr
XM_006724583.4:c.2666T>C	XP_006724646.1:p.Ile889Thr
XM_006724584.3:c.2666T>C	XP_006724647.1:p.Ile889Thr
XM_011530773.2:c.1859T>C	XP_011529075.1:p.Ile620Thr
XM_011530774.3:c.2666T>C	XP_011529076.1:p.Ile889Thr
XM_011530776.2:c.2666T>C	XP_011529078.1:p.Ile889Thr
XM_011530777.2:c.2666T>C	XP_011529079.1:p.Ile889Thr
XM_017029359.2:c.2540T>C	XP_016884848.1:p.Ile847Thr
XM_017029360.1:c.2072T>C	XP_016884849.1:p.Ile691Thr
XR_938365.2:n.2887T>C
NM_001111125.3:c.2570T>C MANE Select	NP_001104595.1:p.Ile857Thr
NM_015075.2:c.1955T>C	NP_055890.1:p.Ile652Thr