Canonical Allele Identifier: CA2429772821
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53241862G= , CM000685.2:g.53241862G= GRCh38
NC_000023.10:g.53271044G= , CM000685.1:g.53271044G= GRCh37
NC_000023.9:g.53287769G= NCBI36
NG_021296.1:g.84479C=
NG_021296.2:g.84489C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3096C= ENSP00000516672.1:p.Tyr1032=
ENST00000638521.1:c.889C=
ENST00000638869.1:c.398C=
ENST00000639642.1:c.227C=
ENST00000640694.1:c.2937C= ENSP00000492403.1:p.Tyr979=
ENST00000642864.1:c.2937C= MANE Select ENSP00000495726.1:p.Tyr979=
ENST00000674510.1:c.2937C= ENSP00000502054.1:p.Tyr979=
ENST00000674761.1:n.1244C=
ENST00000675719.1:c.2907C= ENSP00000501927.1:p.Tyr969=
ENST00000375365.2:c.2322C= ENSP00000364514.2:p.Tyr774=
ENST00000396435.7:c.2937C= ENSP00000379712.3:p.Tyr979=
NM_001111125.2:c.2937C= NP_001104595.1:p.Tyr979=
NM_015075.1:c.2322C= NP_055890.1:p.Tyr774=
XM_006724579.2:c.3033C= XP_006724642.1:p.Tyr1011=
XM_006724580.2:c.2322C= XP_006724643.1:p.Tyr774=
XM_006724581.2:c.3033C= XP_006724644.1:p.Tyr1011=
XM_006724582.2:c.3033C= XP_006724645.1:p.Tyr1011=
XM_006724583.2:c.3033C= XP_006724646.1:p.Tyr1011=
XM_006724584.2:c.3033C= XP_006724647.1:p.Tyr1011=
XM_011530772.1:c.2259C= XP_011529074.1:p.Tyr753=
XM_011530773.1:c.2226C= XP_011529075.1:p.Tyr742=
XM_011530774.1:c.3033C= XP_011529076.1:p.Tyr1011=
XM_011530775.1:c.3033C= XP_011529077.1:p.Tyr1011=
XM_011530776.1:c.3033C= XP_011529078.1:p.Tyr1011=
XM_011530777.1:c.3033C= XP_011529079.1:p.Tyr1011=
XR_938365.1:n.3260C=
XM_006724579.3:c.3033C= XP_006724642.1:p.Tyr1011=
XM_006724580.3:c.2322C= XP_006724643.1:p.Tyr774=
XM_006724581.4:c.3033C= XP_006724644.1:p.Tyr1011=
XM_006724582.4:c.3033C= XP_006724645.1:p.Tyr1011=
XM_006724583.4:c.3033C= XP_006724646.1:p.Tyr1011=
XM_006724584.3:c.3033C= XP_006724647.1:p.Tyr1011=
XM_011530773.2:c.2226C= XP_011529075.1:p.Tyr742=
XM_011530774.3:c.3033C= XP_011529076.1:p.Tyr1011=
XM_011530776.2:c.3033C= XP_011529078.1:p.Tyr1011=
XM_011530777.2:c.3033C= XP_011529079.1:p.Tyr1011=
XM_017029359.2:c.2907C= XP_016884848.1:p.Tyr969=
XM_017029360.1:c.2439C= XP_016884849.1:p.Tyr813=
XR_938365.2:n.3254C=
NM_001111125.3:c.2937C= MANE Select NP_001104595.1:p.Tyr979=
NM_015075.2:c.2322C= NP_055890.1:p.Tyr774=