Canonical Allele Identifier: CA2429772802
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53241771A= , CM000685.2:g.53241771A= GRCh38
NC_000023.10:g.53270953A= , CM000685.1:g.53270953A= GRCh37
NC_000023.9:g.53287678A= NCBI36
NG_021296.1:g.84570T=
NG_021296.2:g.84580T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3174+13T= ENSP00000516672.1:n.3174+13T=
ENST00000638521.1:c.967+13T=
ENST00000638869.1:c.476+13T=
ENST00000639642.1:c.305+13T=
ENST00000640005.1:c.78+13T= ENSP00000491293.1:n.78+13T=
ENST00000640694.1:c.3015+13T= ENSP00000492403.1:n.3015+13T=
ENST00000642864.1:c.3015+13T= MANE Select ENSP00000495726.1:n.3015+13T=
ENST00000674510.1:c.3015+13T= ENSP00000502054.1:n.3015+13T=
ENST00000674761.1:n.1335T=
ENST00000675719.1:c.2985+13T= ENSP00000501927.1:n.2985+13T=
ENST00000375365.2:c.2400+13T= ENSP00000364514.2:n.2400+13T=
ENST00000396435.7:c.3015+13T= ENSP00000379712.3:n.3015+13T=
NM_001111125.2:c.3015+13T= NP_001104595.1:n.3015+13T=
NM_015075.1:c.2400+13T= NP_055890.1:n.2400+13T=
XM_006724579.2:c.3111+13T= XP_006724642.1:n.3111+13T=
XM_006724580.2:c.2400+13T= XP_006724643.1:n.2400+13T=
XM_006724581.2:c.3111+13T= XP_006724644.1:n.3111+13T=
XM_006724582.2:c.3111+13T= XP_006724645.1:n.3111+13T=
XM_006724583.2:c.3111+13T= XP_006724646.1:n.3111+13T=
XM_006724584.2:c.3111+13T= XP_006724647.1:n.3111+13T=
XM_011530772.1:c.2337+13T= XP_011529074.1:n.2337+13T=
XM_011530773.1:c.2304+13T= XP_011529075.1:n.2304+13T=
XM_011530774.1:c.3111+13T= XP_011529076.1:n.3111+13T=
XM_011530775.1:c.3111+13T= XP_011529077.1:n.3111+13T=
XM_011530776.1:c.3111+13T= XP_011529078.1:n.3111+13T=
XM_011530777.1:c.3111+13T= XP_011529079.1:n.3111+13T=
XR_938365.1:n.3338+13T=
XM_006724579.3:c.3111+13T= XP_006724642.1:n.3111+13T=
XM_006724580.3:c.2400+13T= XP_006724643.1:n.2400+13T=
XM_006724581.4:c.3111+13T= XP_006724644.1:n.3111+13T=
XM_006724582.4:c.3111+13T= XP_006724645.1:n.3111+13T=
XM_006724583.4:c.3111+13T= XP_006724646.1:n.3111+13T=
XM_006724584.3:c.3111+13T= XP_006724647.1:n.3111+13T=
XM_011530773.2:c.2304+13T= XP_011529075.1:n.2304+13T=
XM_011530774.3:c.3111+13T= XP_011529076.1:n.3111+13T=
XM_011530776.2:c.3111+13T= XP_011529078.1:n.3111+13T=
XM_011530777.2:c.3111+13T= XP_011529079.1:n.3111+13T=
XM_017029359.2:c.2985+13T= XP_016884848.1:n.2985+13T=
XM_017029360.1:c.2517+13T= XP_016884849.1:n.2517+13T=
XR_938365.2:n.3332+13T=
NM_001111125.3:c.3015+13T= MANE Select NP_001104595.1:n.3015+13T=
NM_015075.2:c.2400+13T= NP_055890.1:n.2400+13T=