Canonical Allele Identifier: CA516674125

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53279928T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250746T>A , CM000685.2:g.53250746T>A	GRCh38
NC_000023.10:g.53279928T>A , CM000685.1:g.53279928T>A	GRCh37
NC_000023.9:g.53296653T>A	NCBI36
NG_021296.1:g.75595A>T
NG_021296.2:g.75605A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1989A>T	ENSP00000516672.1:p.Ser663=
ENST00000640694.1:c.1830A>T	ENSP00000492403.1:p.Ser610=
ENST00000642864.1:c.1830A>T MANE Select	ENSP00000495726.1:p.Ser610=
ENST00000674510.1:c.1830A>T	ENSP00000502054.1:p.Ser610=
ENST00000675719.1:c.1800A>T	ENSP00000501927.1:p.Ser600=
ENST00000375365.2:c.1215A>T	ENSP00000364514.2:p.Ser405=
ENST00000396435.7:c.1830A>T	ENSP00000379712.3:p.Ser610=
NM_001111125.2:c.1830A>T	NP_001104595.1:p.Ser610=
NM_015075.1:c.1215A>T	NP_055890.1:p.Ser405=
XM_006724579.2:c.1926A>T	XP_006724642.1:p.Ser642=
XM_006724580.2:c.1215A>T	XP_006724643.1:p.Ser405=
XM_006724581.2:c.1926A>T	XP_006724644.1:p.Ser642=
XM_006724582.2:c.1926A>T	XP_006724645.1:p.Ser642=
XM_006724583.2:c.1926A>T	XP_006724646.1:p.Ser642=
XM_006724584.2:c.1926A>T	XP_006724647.1:p.Ser642=
XM_011530772.1:c.1152A>T	XP_011529074.1:p.Ser384=
XM_011530773.1:c.1119A>T	XP_011529075.1:p.Ser373=
XM_011530774.1:c.1926A>T	XP_011529076.1:p.Ser642=
XM_011530775.1:c.1926A>T	XP_011529077.1:p.Ser642=
XM_011530776.1:c.1926A>T	XP_011529078.1:p.Ser642=
XM_011530777.1:c.1926A>T	XP_011529079.1:p.Ser642=
XR_938365.1:n.2153A>T
XM_006724579.3:c.1926A>T	XP_006724642.1:p.Ser642=
XM_006724580.3:c.1215A>T	XP_006724643.1:p.Ser405=
XM_006724581.4:c.1926A>T	XP_006724644.1:p.Ser642=
XM_006724582.4:c.1926A>T	XP_006724645.1:p.Ser642=
XM_006724583.4:c.1926A>T	XP_006724646.1:p.Ser642=
XM_006724584.3:c.1926A>T	XP_006724647.1:p.Ser642=
XM_011530773.2:c.1119A>T	XP_011529075.1:p.Ser373=
XM_011530774.3:c.1926A>T	XP_011529076.1:p.Ser642=
XM_011530776.2:c.1926A>T	XP_011529078.1:p.Ser642=
XM_011530777.2:c.1926A>T	XP_011529079.1:p.Ser642=
XM_017029359.2:c.1800A>T	XP_016884848.1:p.Ser600=
XM_017029360.1:c.1332A>T	XP_016884849.1:p.Ser444=
XR_938365.2:n.2147A>T
NM_001111125.3:c.1830A>T MANE Select	NP_001104595.1:p.Ser610=
NM_015075.2:c.1215A>T	NP_055890.1:p.Ser405=