Canonical Allele Identifier: CA413149224

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53271022G>C (hg19) ; chrX:g.53241840G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241840G>C , CM000685.2:g.53241840G>C	GRCh38
NC_000023.10:g.53271022G>C , CM000685.1:g.53271022G>C	GRCh37
NC_000023.9:g.53287747G>C	NCBI36
NG_021296.1:g.84501C>G
NG_021296.2:g.84511C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3118C>G	ENSP00000516672.1:p.Pro1040Ala
ENST00000638521.1:c.911C>G
ENST00000638869.1:c.420C>G
ENST00000639642.1:c.249C>G
ENST00000640005.1:c.22C>G	ENSP00000491293.1:p.Pro8Ala
ENST00000640694.1:c.2959C>G	ENSP00000492403.1:p.Pro987Ala
ENST00000642864.1:c.2959C>G MANE Select	ENSP00000495726.1:p.Pro987Ala
ENST00000674510.1:c.2959C>G	ENSP00000502054.1:p.Pro987Ala
ENST00000674761.1:n.1266C>G
ENST00000675719.1:c.2929C>G	ENSP00000501927.1:p.Pro977Ala
ENST00000375365.2:c.2344C>G	ENSP00000364514.2:p.Pro782Ala
ENST00000396435.7:c.2959C>G	ENSP00000379712.3:p.Pro987Ala
NM_001111125.2:c.2959C>G	NP_001104595.1:p.Pro987Ala
NM_015075.1:c.2344C>G	NP_055890.1:p.Pro782Ala
XM_006724579.2:c.3055C>G	XP_006724642.1:p.Pro1019Ala
XM_006724580.2:c.2344C>G	XP_006724643.1:p.Pro782Ala
XM_006724581.2:c.3055C>G	XP_006724644.1:p.Pro1019Ala
XM_006724582.2:c.3055C>G	XP_006724645.1:p.Pro1019Ala
XM_006724583.2:c.3055C>G	XP_006724646.1:p.Pro1019Ala
XM_006724584.2:c.3055C>G	XP_006724647.1:p.Pro1019Ala
XM_011530772.1:c.2281C>G	XP_011529074.1:p.Pro761Ala
XM_011530773.1:c.2248C>G	XP_011529075.1:p.Pro750Ala
XM_011530774.1:c.3055C>G	XP_011529076.1:p.Pro1019Ala
XM_011530775.1:c.3055C>G	XP_011529077.1:p.Pro1019Ala
XM_011530776.1:c.3055C>G	XP_011529078.1:p.Pro1019Ala
XM_011530777.1:c.3055C>G	XP_011529079.1:p.Pro1019Ala
XR_938365.1:n.3282C>G
XM_006724579.3:c.3055C>G	XP_006724642.1:p.Pro1019Ala
XM_006724580.3:c.2344C>G	XP_006724643.1:p.Pro782Ala
XM_006724581.4:c.3055C>G	XP_006724644.1:p.Pro1019Ala
XM_006724582.4:c.3055C>G	XP_006724645.1:p.Pro1019Ala
XM_006724583.4:c.3055C>G	XP_006724646.1:p.Pro1019Ala
XM_006724584.3:c.3055C>G	XP_006724647.1:p.Pro1019Ala
XM_011530773.2:c.2248C>G	XP_011529075.1:p.Pro750Ala
XM_011530774.3:c.3055C>G	XP_011529076.1:p.Pro1019Ala
XM_011530776.2:c.3055C>G	XP_011529078.1:p.Pro1019Ala
XM_011530777.2:c.3055C>G	XP_011529079.1:p.Pro1019Ala
XM_017029359.2:c.2929C>G	XP_016884848.1:p.Pro977Ala
XM_017029360.1:c.2461C>G	XP_016884849.1:p.Pro821Ala
XR_938365.2:n.3276C>G
NM_001111125.3:c.2959C>G MANE Select	NP_001104595.1:p.Pro987Ala
NM_015075.2:c.2344C>G	NP_055890.1:p.Pro782Ala