Canonical Allele Identifier: CA2820950238

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235130_53235131insGGGGGGGGGCGGGGG , CM000685.2:g.53235130_53235131insGGGGGGGGGCGGGGG	GRCh38
NC_000023.10:g.53264312_53264313insGGGGGGGGGCGGGGG , CM000685.1:g.53264312_53264313insGGGGGGGGGCGGGGG	GRCh37
NC_000023.9:g.53281037_53281038insGGGGGGGGGCGGGGG	NCBI36
NG_021296.1:g.91218_91219insCCCCCCCCCCCCGCC
NG_021296.2:g.91228_91229insCCCCCCCCCCCCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3722_3723insCCCCCCCCCCCCGCC	ENSP00000516672.1:p.Pro1241_Pro1242insProProProProPro
ENST00000638521.1:c.1453+660_1453+661insCCCCCCCCCCCCGCC
ENST00000638869.1:c.962+660_962+661insCCCCCCCCCCCCGCC
ENST00000639796.1:c.316+1199_316+1200insCCCCCCCCCCCCGCC	ENSP00000492252.1:n.316+1199_316+1200insCCCCCCCCCCCCGCC
ENST00000640005.1:c.514+1199_514+1200insCCCCCCCCCCCCGCC	ENSP00000491293.1:n.514+1199_514+1200insCCCCCCCCCCCCGCC
ENST00000640436.1:n.543_544insCCCCCCCCCCCCGCC
ENST00000640694.1:c.*48_*49insCCCCCCCCCCCCGCC	ENSP00000492403.1:n.*48_*49insCCCCCCCCCCCCGCC
ENST00000642864.1:c.3563_3564insCCCCCCCCCCCCGCC MANE Select	ENSP00000495726.1:p.Pro1188_Pro1189insProProProProPro
ENST00000674510.1:c.3563_3564insCCCCCCCCCCCCGCC	ENSP00000502054.1:p.Pro1188_Pro1189insProProProProPro
ENST00000675719.1:c.3533_3534insCCCCCCCCCCCCGCC	ENSP00000501927.1:p.Pro1178_Pro1179insProProProProPro
ENST00000375365.2:c.*48_*49insCCCCCCCCCCCCGCC	ENSP00000364514.2:n.*48_*49insCCCCCCCCCCCCGCC
ENST00000396435.7:c.3563_3564insCCCCCCCCCCCCGCC	ENSP00000379712.3:p.Pro1188_Pro1189insProProProProPro
NM_001111125.2:c.3563_3564insCCCCCCCCCCCCGCC	NP_001104595.1:p.Pro1188_Pro1189insProProProProPro
NM_015075.1:c.*48_*49insCCCCCCCCCCCCGCC	NP_055890.1:n.*48_*49insCCCCCCCCCCCCGCC
XM_006724579.2:c.3659_3660insCCCCCCCCCCCCGCC	XP_006724642.1:p.Pro1220_Pro1221insProProProProPro
XM_006724580.2:c.2948_2949insCCCCCCCCCCCCGCC	XP_006724643.1:p.Pro983_Pro984insProProProProPro
XM_006724581.2:c.3597+660_3597+661insCCCCCCCCCCCCGCC	XP_006724644.1:n.3597+660_3597+661insCCCCCCCCCCCCGCC
XM_006724582.2:c.3597+660_3597+661insCCCCCCCCCCCCGCC	XP_006724645.1:n.3597+660_3597+661insCCCCCCCCCCCCGCC
XM_006724583.2:c.3547+1199_3547+1200insCCCCCCCCCCCCGCC	XP_006724646.1:n.3547+1199_3547+1200insCCCCCCCCCCCCGCC
XM_006724584.2:c.*48_*49insCCCCCCCCCCCCGCC	XP_006724647.1:n.*48_*49insCCCCCCCCCCCCGCC
XM_011530772.1:c.2885_2886insCCCCCCCCCCCCGCC	XP_011529074.1:p.Pro962_Pro963insProProProProPro
XM_011530773.1:c.2852_2853insCCCCCCCCCCCCGCC	XP_011529075.1:p.Pro951_Pro952insProProProProPro
XM_011530775.1:c.3547+1199_3547+1200insCCCCCCCCCCCCGCC	XP_011529077.1:n.3547+1199_3547+1200insCCCCCCCCCCCCGCC
XM_006724579.3:c.3659_3660insCCCCCCCCCCCCGCC	XP_006724642.1:p.Pro1220_Pro1221insProProProProPro
XM_006724580.3:c.2948_2949insCCCCCCCCCCCCGCC	XP_006724643.1:p.Pro983_Pro984insProProProProPro
XM_006724581.4:c.3597+660_3597+661insCCCCCCCCCCCCGCC	XP_006724644.1:n.3597+660_3597+661insCCCCCCCCCCCCGCC
XM_006724582.4:c.3597+660_3597+661insCCCCCCCCCCCCGCC	XP_006724645.1:n.3597+660_3597+661insCCCCCCCCCCCCGCC
XM_006724583.4:c.3547+1199_3547+1200insCCCCCCCCCCCCGCC	XP_006724646.1:n.3547+1199_3547+1200insCCCCCCCCCCCCGCC
XM_006724584.3:c.*48_*49insCCCCCCCCCCCCGCC	XP_006724647.1:n.*48_*49insCCCCCCCCCCCCGCC
XM_011530773.2:c.2852_2853insCCCCCCCCCCCCGCC	XP_011529075.1:p.Pro951_Pro952insProProProProPro
XM_017029359.2:c.3533_3534insCCCCCCCCCCCCGCC	XP_016884848.1:p.Pro1178_Pro1179insProProProProPro
XM_017029360.1:c.3065_3066insCCCCCCCCCCCCGCC	XP_016884849.1:p.Pro1022_Pro1023insProProProProPro
NM_001111125.3:c.3563_3564insCCCCCCCCCCCCGCC MANE Select	NP_001104595.1:p.Pro1188_Pro1189insProProProProPro
NM_015075.2:c.*48_*49insCCCCCCCCCCCCGCC	NP_055890.1:n.*48_*49insCCCCCCCCCCCCGCC