Canonical Allele Identifier: CA2429770704

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235129_53235131delinsGGT , CM000685.2:g.53235129_53235131delinsGGT	GRCh38
NC_000023.10:g.53264311_53264313delinsGGT , CM000685.1:g.53264311_53264313delinsGGT	GRCh37
NC_000023.9:g.53281036_53281038delinsGGT	NCBI36
NG_021296.1:g.91210_91212delinsACC
NG_021296.2:g.91220_91222delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3714_3716delinsACC	ENSP00000516672.1:p.Pro1238=
ENST00000638521.1:c.1453+652_1453+654delinsACC
ENST00000638869.1:c.962+652_962+654delinsACC
ENST00000639796.1:c.316+1191_316+1193delinsACC	ENSP00000492252.1:n.316+1191_316+1193delinsACC
ENST00000640005.1:c.514+1191_514+1193delinsACC	ENSP00000491293.1:n.514+1191_514+1193delinsACC
ENST00000640436.1:n.535_537delinsACC
ENST00000640694.1:c.*40_*42delinsACC	ENSP00000492403.1:n.*40_*42delinsACC
ENST00000642864.1:c.3555_3557delinsACC MANE Select	ENSP00000495726.1:p.Pro1185=
ENST00000674510.1:c.3555_3557delinsACC	ENSP00000502054.1:p.Pro1185=
ENST00000675719.1:c.3525_3527delinsACC	ENSP00000501927.1:p.Pro1175=
ENST00000375365.2:c.*40_*42delinsACC	ENSP00000364514.2:n.*40_*42delinsACC
ENST00000396435.7:c.3555_3557delinsACC	ENSP00000379712.3:p.Pro1185=
NM_001111125.2:c.3555_3557delinsACC	NP_001104595.1:p.Pro1185=
NM_015075.1:c.*40_*42delinsACC	NP_055890.1:n.*40_*42delinsACC
XM_006724579.2:c.3651_3653delinsACC	XP_006724642.1:p.Pro1217=
XM_006724580.2:c.2940_2942delinsACC	XP_006724643.1:p.Pro980=
XM_006724581.2:c.3597+652_3597+654delinsACC	XP_006724644.1:n.3597+652_3597+654delinsACC
XM_006724582.2:c.3597+652_3597+654delinsACC	XP_006724645.1:n.3597+652_3597+654delinsACC
XM_006724583.2:c.3547+1191_3547+1193delinsACC	XP_006724646.1:n.3547+1191_3547+1193delinsACC
XM_006724584.2:c.*40_*42delinsACC	XP_006724647.1:n.*40_*42delinsACC
XM_011530772.1:c.2877_2879delinsACC	XP_011529074.1:p.Pro959=
XM_011530773.1:c.2844_2846delinsACC	XP_011529075.1:p.Pro948=
XM_011530775.1:c.3547+1191_3547+1193delinsACC	XP_011529077.1:n.3547+1191_3547+1193delinsACC
XM_006724579.3:c.3651_3653delinsACC	XP_006724642.1:p.Pro1217=
XM_006724580.3:c.2940_2942delinsACC	XP_006724643.1:p.Pro980=
XM_006724581.4:c.3597+652_3597+654delinsACC	XP_006724644.1:n.3597+652_3597+654delinsACC
XM_006724582.4:c.3597+652_3597+654delinsACC	XP_006724645.1:n.3597+652_3597+654delinsACC
XM_006724583.4:c.3547+1191_3547+1193delinsACC	XP_006724646.1:n.3547+1191_3547+1193delinsACC
XM_006724584.3:c.*40_*42delinsACC	XP_006724647.1:n.*40_*42delinsACC
XM_011530773.2:c.2844_2846delinsACC	XP_011529075.1:p.Pro948=
XM_017029359.2:c.3525_3527delinsACC	XP_016884848.1:p.Pro1175=
XM_017029360.1:c.3057_3059delinsACC	XP_016884849.1:p.Pro1019=
NM_001111125.3:c.3555_3557delinsACC MANE Select	NP_001104595.1:p.Pro1185=
NM_015075.2:c.*40_*42delinsACC	NP_055890.1:n.*40_*42delinsACC