Canonical Allele Identifier: CA516674604

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53285192A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53256010A>C , CM000685.2:g.53256010A>C	GRCh38
NC_000023.10:g.53285192A>C , CM000685.1:g.53285192A>C	GRCh37
NC_000023.9:g.53301917A>C	NCBI36
NG_021296.1:g.70331T>G
NG_021296.2:g.70341T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.948T>G	ENSP00000516672.1:p.Pro316=
ENST00000638630.1:c.78T>G	ENSP00000492390.1:p.Pro26=
ENST00000640694.1:c.789T>G	ENSP00000492403.1:p.Pro263=
ENST00000642864.1:c.789T>G MANE Select	ENSP00000495726.1:p.Pro263=
ENST00000674510.1:c.789T>G	ENSP00000502054.1:p.Pro263=
ENST00000675719.1:c.759T>G	ENSP00000501927.1:p.Pro253=
ENST00000375365.2:c.174T>G	ENSP00000364514.2:p.Pro58=
ENST00000396435.7:c.789T>G	ENSP00000379712.3:p.Pro263=
NM_001111125.2:c.789T>G	NP_001104595.1:p.Pro263=
NM_015075.1:c.174T>G	NP_055890.1:p.Pro58=
XM_006724579.2:c.885T>G	XP_006724642.1:p.Pro295=
XM_006724580.2:c.174T>G	XP_006724643.1:p.Pro58=
XM_006724581.2:c.885T>G	XP_006724644.1:p.Pro295=
XM_006724582.2:c.885T>G	XP_006724645.1:p.Pro295=
XM_006724583.2:c.885T>G	XP_006724646.1:p.Pro295=
XM_006724584.2:c.885T>G	XP_006724647.1:p.Pro295=
XM_011530772.1:c.111T>G	XP_011529074.1:p.Pro37=
XM_011530773.1:c.78T>G	XP_011529075.1:p.Pro26=
XM_011530774.1:c.885T>G	XP_011529076.1:p.Pro295=
XM_011530775.1:c.885T>G	XP_011529077.1:p.Pro295=
XM_011530776.1:c.885T>G	XP_011529078.1:p.Pro295=
XM_011530777.1:c.885T>G	XP_011529079.1:p.Pro295=
XR_938365.1:n.1112T>G
XM_006724579.3:c.885T>G	XP_006724642.1:p.Pro295=
XM_006724580.3:c.174T>G	XP_006724643.1:p.Pro58=
XM_006724581.4:c.885T>G	XP_006724644.1:p.Pro295=
XM_006724582.4:c.885T>G	XP_006724645.1:p.Pro295=
XM_006724583.4:c.885T>G	XP_006724646.1:p.Pro295=
XM_006724584.3:c.885T>G	XP_006724647.1:p.Pro295=
XM_011530773.2:c.78T>G	XP_011529075.1:p.Pro26=
XM_011530774.3:c.885T>G	XP_011529076.1:p.Pro295=
XM_011530776.2:c.885T>G	XP_011529078.1:p.Pro295=
XM_011530777.2:c.885T>G	XP_011529079.1:p.Pro295=
XM_017029359.2:c.759T>G	XP_016884848.1:p.Pro253=
XM_017029360.1:c.291T>G	XP_016884849.1:p.Pro97=
XR_938365.2:n.1106T>G
NM_001111125.3:c.789T>G MANE Select	NP_001104595.1:p.Pro263=
NM_015075.2:c.174T>G	NP_055890.1:p.Pro58=