Canonical Allele Identifier: CA2429774924
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53248171G= , CM000685.2:g.53248171G= GRCh38
NC_000023.10:g.53277353G= , CM000685.1:g.53277353G= GRCh37
NC_000023.9:g.53294078G= NCBI36
NG_021296.1:g.78170C=
NG_021296.2:g.78180C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.2684C= ENSP00000516672.1:p.Ser895=
ENST00000638521.1:c.477C=
ENST00000640694.1:c.2525C= ENSP00000492403.1:p.Ser842=
ENST00000642864.1:c.2525C= MANE Select ENSP00000495726.1:p.Ser842=
ENST00000674510.1:c.2525C= ENSP00000502054.1:p.Ser842=
ENST00000674761.1:n.276C=
ENST00000675719.1:c.2495C= ENSP00000501927.1:p.Ser832=
ENST00000375365.2:c.1910C= ENSP00000364514.2:p.Ser637=
ENST00000396435.7:c.2525C= ENSP00000379712.3:p.Ser842=
NM_001111125.2:c.2525C= NP_001104595.1:p.Ser842=
NM_015075.1:c.1910C= NP_055890.1:p.Ser637=
XM_006724579.2:c.2621C= XP_006724642.1:p.Ser874=
XM_006724580.2:c.1910C= XP_006724643.1:p.Ser637=
XM_006724581.2:c.2621C= XP_006724644.1:p.Ser874=
XM_006724582.2:c.2621C= XP_006724645.1:p.Ser874=
XM_006724583.2:c.2621C= XP_006724646.1:p.Ser874=
XM_006724584.2:c.2621C= XP_006724647.1:p.Ser874=
XM_011530772.1:c.1847C= XP_011529074.1:p.Ser616=
XM_011530773.1:c.1814C= XP_011529075.1:p.Ser605=
XM_011530774.1:c.2621C= XP_011529076.1:p.Ser874=
XM_011530775.1:c.2621C= XP_011529077.1:p.Ser874=
XM_011530776.1:c.2621C= XP_011529078.1:p.Ser874=
XM_011530777.1:c.2621C= XP_011529079.1:p.Ser874=
XR_938365.1:n.2848C=
XM_006724579.3:c.2621C= XP_006724642.1:p.Ser874=
XM_006724580.3:c.1910C= XP_006724643.1:p.Ser637=
XM_006724581.4:c.2621C= XP_006724644.1:p.Ser874=
XM_006724582.4:c.2621C= XP_006724645.1:p.Ser874=
XM_006724583.4:c.2621C= XP_006724646.1:p.Ser874=
XM_006724584.3:c.2621C= XP_006724647.1:p.Ser874=
XM_011530773.2:c.1814C= XP_011529075.1:p.Ser605=
XM_011530774.3:c.2621C= XP_011529076.1:p.Ser874=
XM_011530776.2:c.2621C= XP_011529078.1:p.Ser874=
XM_011530777.2:c.2621C= XP_011529079.1:p.Ser874=
XM_017029359.2:c.2495C= XP_016884848.1:p.Ser832=
XM_017029360.1:c.2027C= XP_016884849.1:p.Ser676=
XR_938365.2:n.2842C=
NM_001111125.3:c.2525C= MANE Select NP_001104595.1:p.Ser842=
NM_015075.2:c.1910C= NP_055890.1:p.Ser637=