Canonical Allele Identifier: CA2429770764
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53235321G= , CM000685.2:g.53235321G= GRCh38
NC_000023.10:g.53264503G= , CM000685.1:g.53264503G= GRCh37
NC_000023.9:g.53281228G= NCBI36
NG_021296.1:g.91020C=
NG_021296.2:g.91030C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3661-137C= ENSP00000516672.1:n.3661-137C=
ENST00000638521.1:c.1453+462C=
ENST00000638869.1:c.962+462C=
ENST00000639796.1:c.316+1001C= ENSP00000492252.1:n.316+1001C=
ENST00000640005.1:c.514+1001C= ENSP00000491293.1:n.514+1001C=
ENST00000640436.1:n.482-137C=
ENST00000640694.1:c.3452-137C= ENSP00000492403.1:n.3452-137C=
ENST00000642864.1:c.3502-137C= MANE Select ENSP00000495726.1:n.3502-137C=
ENST00000674510.1:c.3502-137C= ENSP00000502054.1:n.3502-137C=
ENST00000675719.1:c.3472-137C= ENSP00000501927.1:n.3472-137C=
ENST00000375365.2:c.2837-137C= ENSP00000364514.2:n.2837-137C=
ENST00000396435.7:c.3502-137C= ENSP00000379712.3:n.3502-137C=
NM_001111125.2:c.3502-137C= NP_001104595.1:n.3502-137C=
NM_015075.1:c.2837-137C= NP_055890.1:n.2837-137C=
XM_006724579.2:c.3598-137C= XP_006724642.1:n.3598-137C=
XM_006724580.2:c.2887-137C= XP_006724643.1:n.2887-137C=
XM_006724581.2:c.3597+462C= XP_006724644.1:n.3597+462C=
XM_006724582.2:c.3597+462C= XP_006724645.1:n.3597+462C=
XM_006724583.2:c.3547+1001C= XP_006724646.1:n.3547+1001C=
XM_006724584.2:c.3548-137C= XP_006724647.1:n.3548-137C=
XM_011530772.1:c.2824-137C= XP_011529074.1:n.2824-137C=
XM_011530773.1:c.2791-137C= XP_011529075.1:n.2791-137C=
XM_011530774.1:c.*166C= XP_011529076.1:n.*166C=
XM_011530775.1:c.3547+1001C= XP_011529077.1:n.3547+1001C=
XM_006724579.3:c.3598-137C= XP_006724642.1:n.3598-137C=
XM_006724580.3:c.2887-137C= XP_006724643.1:n.2887-137C=
XM_006724581.4:c.3597+462C= XP_006724644.1:n.3597+462C=
XM_006724582.4:c.3597+462C= XP_006724645.1:n.3597+462C=
XM_006724583.4:c.3547+1001C= XP_006724646.1:n.3547+1001C=
XM_006724584.3:c.3548-137C= XP_006724647.1:n.3548-137C=
XM_011530773.2:c.2791-137C= XP_011529075.1:n.2791-137C=
XM_011530774.3:c.*166C= XP_011529076.1:n.*166C=
XM_017029359.2:c.3472-137C= XP_016884848.1:n.3472-137C=
XM_017029360.1:c.3004-137C= XP_016884849.1:n.3004-137C=
NM_001111125.3:c.3502-137C= MANE Select NP_001104595.1:n.3502-137C=
NM_015075.2:c.2837-137C= NP_055890.1:n.2837-137C=