Canonical Allele Identifier: CA641903975

Gene: IQSEC2

Linked Data

• dbSNP Id: rs1602258056
• gnomAD v2: X-53264307-C-CGGGGGGGGG
• gnomAD v4: X-53235125-C-CGGGGGGGGG
• MyVariant Identifiers: chrX:g.53264307_53264308insGGGGGGGGG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235130_53235131insGGGGGGGGG , CM000685.2:g.53235130_53235131insGGGGGGGGG	GRCh38
NC_000023.10:g.53264312_53264313insGGGGGGGGG , CM000685.1:g.53264312_53264313insGGGGGGGGG	GRCh37
NC_000023.9:g.53281037_53281038insGGGGGGGGG	NCBI36
NG_021296.1:g.91215_91216insCCCCCCCCC
NG_021296.2:g.91225_91226insCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3719_3720insCCCCCCCCC	ENSP00000516672.1:p.Pro1240_Pro1241insProProPro
ENST00000638521.1:c.1453+657_1453+658insCCCCCCCCC
ENST00000638869.1:c.962+657_962+658insCCCCCCCCC
ENST00000639796.1:c.316+1196_316+1197insCCCCCCCCC	ENSP00000492252.1:n.316+1196_316+1197insCCCCCCCCC
ENST00000640005.1:c.514+1196_514+1197insCCCCCCCCC	ENSP00000491293.1:n.514+1196_514+1197insCCCCCCCCC
ENST00000640436.1:n.540_541insCCCCCCCCC
ENST00000640694.1:c.*45_*46insCCCCCCCCC	ENSP00000492403.1:n.*45_*46insCCCCCCCCC
ENST00000642864.1:c.3560_3561insCCCCCCCCC MANE Select	ENSP00000495726.1:p.Pro1187_Pro1188insProProPro
ENST00000674510.1:c.3560_3561insCCCCCCCCC	ENSP00000502054.1:p.Pro1187_Pro1188insProProPro
ENST00000675719.1:c.3530_3531insCCCCCCCCC	ENSP00000501927.1:p.Pro1177_Pro1178insProProPro
ENST00000375365.2:c.*45_*46insCCCCCCCCC	ENSP00000364514.2:n.*45_*46insCCCCCCCCC
ENST00000396435.7:c.3560_3561insCCCCCCCCC	ENSP00000379712.3:p.Pro1187_Pro1188insProProPro
NM_001111125.2:c.3560_3561insCCCCCCCCC	NP_001104595.1:p.Pro1187_Pro1188insProProPro
NM_015075.1:c.*45_*46insCCCCCCCCC	NP_055890.1:n.*45_*46insCCCCCCCCC
XM_006724579.2:c.3656_3657insCCCCCCCCC	XP_006724642.1:p.Pro1219_Pro1220insProProPro
XM_006724580.2:c.2945_2946insCCCCCCCCC	XP_006724643.1:p.Pro982_Pro983insProProPro
XM_006724581.2:c.3597+657_3597+658insCCCCCCCCC	XP_006724644.1:n.3597+657_3597+658insCCCCCCCCC
XM_006724582.2:c.3597+657_3597+658insCCCCCCCCC	XP_006724645.1:n.3597+657_3597+658insCCCCCCCCC
XM_006724583.2:c.3547+1196_3547+1197insCCCCCCCCC	XP_006724646.1:n.3547+1196_3547+1197insCCCCCCCCC
XM_006724584.2:c.*45_*46insCCCCCCCCC	XP_006724647.1:n.*45_*46insCCCCCCCCC
XM_011530772.1:c.2882_2883insCCCCCCCCC	XP_011529074.1:p.Pro961_Pro962insProProPro
XM_011530773.1:c.2849_2850insCCCCCCCCC	XP_011529075.1:p.Pro950_Pro951insProProPro
XM_011530775.1:c.3547+1196_3547+1197insCCCCCCCCC	XP_011529077.1:n.3547+1196_3547+1197insCCCCCCCCC
XM_006724579.3:c.3656_3657insCCCCCCCCC	XP_006724642.1:p.Pro1219_Pro1220insProProPro
XM_006724580.3:c.2945_2946insCCCCCCCCC	XP_006724643.1:p.Pro982_Pro983insProProPro
XM_006724581.4:c.3597+657_3597+658insCCCCCCCCC	XP_006724644.1:n.3597+657_3597+658insCCCCCCCCC
XM_006724582.4:c.3597+657_3597+658insCCCCCCCCC	XP_006724645.1:n.3597+657_3597+658insCCCCCCCCC
XM_006724583.4:c.3547+1196_3547+1197insCCCCCCCCC	XP_006724646.1:n.3547+1196_3547+1197insCCCCCCCCC
XM_006724584.3:c.*45_*46insCCCCCCCCC	XP_006724647.1:n.*45_*46insCCCCCCCCC
XM_011530773.2:c.2849_2850insCCCCCCCCC	XP_011529075.1:p.Pro950_Pro951insProProPro
XM_017029359.2:c.3530_3531insCCCCCCCCC	XP_016884848.1:p.Pro1177_Pro1178insProProPro
XM_017029360.1:c.3062_3063insCCCCCCCCC	XP_016884849.1:p.Pro1021_Pro1022insProProPro
NM_001111125.3:c.3560_3561insCCCCCCCCC MANE Select	NP_001104595.1:p.Pro1187_Pro1188insProProPro
NM_015075.2:c.*45_*46insCCCCCCCCC	NP_055890.1:n.*45_*46insCCCCCCCCC