Canonical Allele Identifier: CA641903980

Gene: IQSEC2

Linked Data

• gnomAD v2: X-53264313-T-TGGGGGG
• gnomAD v3: X-53235131-T-TGGGGGG
• gnomAD v4: X-53235131-T-TGGGGGG
• MyVariant Identifiers: chrX:g.53264313_53264314insGGGGGG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235136_53235137insGGGGGG , CM000685.2:g.53235136_53235137insGGGGGG	GRCh38
NC_000023.10:g.53264318_53264319insGGGGGG , CM000685.1:g.53264318_53264319insGGGGGG	GRCh37
NC_000023.9:g.53281043_53281044insGGGGGG	NCBI36
NG_021296.1:g.91209_91210insCCCCCC
NG_021296.2:g.91219_91220insCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3713_3714insCCCCCC	ENSP00000516672.1:p.Pro1238_Pro1239insProPro
ENST00000638521.1:c.1453+651_1453+652insCCCCCC
ENST00000638869.1:c.962+651_962+652insCCCCCC
ENST00000639796.1:c.316+1190_316+1191insCCCCCC	ENSP00000492252.1:n.316+1190_316+1191insCCCCCC
ENST00000640005.1:c.514+1190_514+1191insCCCCCC	ENSP00000491293.1:n.514+1190_514+1191insCCCCCC
ENST00000640436.1:n.534_535insCCCCCC
ENST00000640694.1:c.*39_*40insCCCCCC	ENSP00000492403.1:n.*39_*40insCCCCCC
ENST00000642864.1:c.3554_3555insCCCCCC MANE Select	ENSP00000495726.1:p.Pro1185_Pro1186insProPro
ENST00000674510.1:c.3554_3555insCCCCCC	ENSP00000502054.1:p.Pro1185_Pro1186insProPro
ENST00000675719.1:c.3524_3525insCCCCCC	ENSP00000501927.1:p.Pro1175_Pro1176insProPro
ENST00000375365.2:c.*39_*40insCCCCCC	ENSP00000364514.2:n.*39_*40insCCCCCC
ENST00000396435.7:c.3554_3555insCCCCCC	ENSP00000379712.3:p.Pro1185_Pro1186insProPro
NM_001111125.2:c.3554_3555insCCCCCC	NP_001104595.1:p.Pro1185_Pro1186insProPro
NM_015075.1:c.*39_*40insCCCCCC	NP_055890.1:n.*39_*40insCCCCCC
XM_006724579.2:c.3650_3651insCCCCCC	XP_006724642.1:p.Pro1217_Pro1218insProPro
XM_006724580.2:c.2939_2940insCCCCCC	XP_006724643.1:p.Pro980_Pro981insProPro
XM_006724581.2:c.3597+651_3597+652insCCCCCC	XP_006724644.1:n.3597+651_3597+652insCCCCCC
XM_006724582.2:c.3597+651_3597+652insCCCCCC	XP_006724645.1:n.3597+651_3597+652insCCCCCC
XM_006724583.2:c.3547+1190_3547+1191insCCCCCC	XP_006724646.1:n.3547+1190_3547+1191insCCCCCC
XM_006724584.2:c.*39_*40insCCCCCC	XP_006724647.1:n.*39_*40insCCCCCC
XM_011530772.1:c.2876_2877insCCCCCC	XP_011529074.1:p.Pro959_Pro960insProPro
XM_011530773.1:c.2843_2844insCCCCCC	XP_011529075.1:p.Pro948_Pro949insProPro
XM_011530775.1:c.3547+1190_3547+1191insCCCCCC	XP_011529077.1:n.3547+1190_3547+1191insCCCCCC
XM_006724579.3:c.3650_3651insCCCCCC	XP_006724642.1:p.Pro1217_Pro1218insProPro
XM_006724580.3:c.2939_2940insCCCCCC	XP_006724643.1:p.Pro980_Pro981insProPro
XM_006724581.4:c.3597+651_3597+652insCCCCCC	XP_006724644.1:n.3597+651_3597+652insCCCCCC
XM_006724582.4:c.3597+651_3597+652insCCCCCC	XP_006724645.1:n.3597+651_3597+652insCCCCCC
XM_006724583.4:c.3547+1190_3547+1191insCCCCCC	XP_006724646.1:n.3547+1190_3547+1191insCCCCCC
XM_006724584.3:c.*39_*40insCCCCCC	XP_006724647.1:n.*39_*40insCCCCCC
XM_011530773.2:c.2843_2844insCCCCCC	XP_011529075.1:p.Pro948_Pro949insProPro
XM_017029359.2:c.3524_3525insCCCCCC	XP_016884848.1:p.Pro1175_Pro1176insProPro
XM_017029360.1:c.3056_3057insCCCCCC	XP_016884849.1:p.Pro1019_Pro1020insProPro
NM_001111125.3:c.3554_3555insCCCCCC MANE Select	NP_001104595.1:p.Pro1185_Pro1186insProPro
NM_015075.2:c.*39_*40insCCCCCC	NP_055890.1:n.*39_*40insCCCCCC