Canonical Allele Identifier: CA2429770625
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53234869G= , CM000685.2:g.53234869G= GRCh38
NC_000023.10:g.53264051G= , CM000685.1:g.53264051G= GRCh37
NC_000023.9:g.53280776G= NCBI36
NG_021296.1:g.91472C=
NG_021296.2:g.91482C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3976C= ENSP00000516672.1:p.Gln1326=
ENST00000638521.1:c.1453+914C=
ENST00000638869.1:c.962+914C=
ENST00000639796.1:c.316+1453C= ENSP00000492252.1:n.316+1453C=
ENST00000640005.1:c.514+1453C= ENSP00000491293.1:n.514+1453C=
ENST00000640694.1:c.*302C= ENSP00000492403.1:n.*302C=
ENST00000642864.1:c.3817C= MANE Select ENSP00000495726.1:p.Gln1273=
ENST00000674510.1:c.3817C= ENSP00000502054.1:p.Gln1273=
ENST00000675719.1:c.3787C= ENSP00000501927.1:p.Gln1263=
ENST00000375365.2:c.*302C= ENSP00000364514.2:n.*302C=
ENST00000396435.7:c.3817C= ENSP00000379712.3:p.Gln1273=
NM_001111125.2:c.3817C= NP_001104595.1:p.Gln1273=
NM_015075.1:c.*302C= NP_055890.1:n.*302C=
XM_006724579.2:c.3913C= XP_006724642.1:p.Gln1305=
XM_006724580.2:c.3202C= XP_006724643.1:p.Gln1068=
XM_006724581.2:c.3597+914C= XP_006724644.1:n.3597+914C=
XM_006724582.2:c.3597+914C= XP_006724645.1:n.3597+914C=
XM_006724583.2:c.3547+1453C= XP_006724646.1:n.3547+1453C=
XM_006724584.2:c.*302C= XP_006724647.1:n.*302C=
XM_011530772.1:c.3139C= XP_011529074.1:p.Gln1047=
XM_011530773.1:c.3106C= XP_011529075.1:p.Gln1036=
XM_011530775.1:c.3547+1453C= XP_011529077.1:n.3547+1453C=
XM_006724579.3:c.3913C= XP_006724642.1:p.Gln1305=
XM_006724580.3:c.3202C= XP_006724643.1:p.Gln1068=
XM_006724581.4:c.3597+914C= XP_006724644.1:n.3597+914C=
XM_006724582.4:c.3597+914C= XP_006724645.1:n.3597+914C=
XM_006724583.4:c.3547+1453C= XP_006724646.1:n.3547+1453C=
XM_006724584.3:c.*302C= XP_006724647.1:n.*302C=
XM_011530773.2:c.3106C= XP_011529075.1:p.Gln1036=
XM_017029359.2:c.3787C= XP_016884848.1:p.Gln1263=
XM_017029360.1:c.3319C= XP_016884849.1:p.Gln1107=
NM_001111125.3:c.3817C= MANE Select NP_001104595.1:p.Gln1273=
NM_015075.2:c.*302C= NP_055890.1:n.*302C=