Canonical Allele Identifier: CA2429772817
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53241847T= , CM000685.2:g.53241847T= GRCh38
NC_000023.10:g.53271029T= , CM000685.1:g.53271029T= GRCh37
NC_000023.9:g.53287754T= NCBI36
NG_021296.1:g.84494A=
NG_021296.2:g.84504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3111A= ENSP00000516672.1:p.Pro1037=
ENST00000638521.1:c.904A=
ENST00000638869.1:c.413A=
ENST00000639642.1:c.242A=
ENST00000640005.1:c.15A= ENSP00000491293.1:p.Pro5=
ENST00000640694.1:c.2952A= ENSP00000492403.1:p.Pro984=
ENST00000642864.1:c.2952A= MANE Select ENSP00000495726.1:p.Pro984=
ENST00000674510.1:c.2952A= ENSP00000502054.1:p.Pro984=
ENST00000674761.1:n.1259A=
ENST00000675719.1:c.2922A= ENSP00000501927.1:p.Pro974=
ENST00000375365.2:c.2337A= ENSP00000364514.2:p.Pro779=
ENST00000396435.7:c.2952A= ENSP00000379712.3:p.Pro984=
NM_001111125.2:c.2952A= NP_001104595.1:p.Pro984=
NM_015075.1:c.2337A= NP_055890.1:p.Pro779=
XM_006724579.2:c.3048A= XP_006724642.1:p.Pro1016=
XM_006724580.2:c.2337A= XP_006724643.1:p.Pro779=
XM_006724581.2:c.3048A= XP_006724644.1:p.Pro1016=
XM_006724582.2:c.3048A= XP_006724645.1:p.Pro1016=
XM_006724583.2:c.3048A= XP_006724646.1:p.Pro1016=
XM_006724584.2:c.3048A= XP_006724647.1:p.Pro1016=
XM_011530772.1:c.2274A= XP_011529074.1:p.Pro758=
XM_011530773.1:c.2241A= XP_011529075.1:p.Pro747=
XM_011530774.1:c.3048A= XP_011529076.1:p.Pro1016=
XM_011530775.1:c.3048A= XP_011529077.1:p.Pro1016=
XM_011530776.1:c.3048A= XP_011529078.1:p.Pro1016=
XM_011530777.1:c.3048A= XP_011529079.1:p.Pro1016=
XR_938365.1:n.3275A=
XM_006724579.3:c.3048A= XP_006724642.1:p.Pro1016=
XM_006724580.3:c.2337A= XP_006724643.1:p.Pro779=
XM_006724581.4:c.3048A= XP_006724644.1:p.Pro1016=
XM_006724582.4:c.3048A= XP_006724645.1:p.Pro1016=
XM_006724583.4:c.3048A= XP_006724646.1:p.Pro1016=
XM_006724584.3:c.3048A= XP_006724647.1:p.Pro1016=
XM_011530773.2:c.2241A= XP_011529075.1:p.Pro747=
XM_011530774.3:c.3048A= XP_011529076.1:p.Pro1016=
XM_011530776.2:c.3048A= XP_011529078.1:p.Pro1016=
XM_011530777.2:c.3048A= XP_011529079.1:p.Pro1016=
XM_017029359.2:c.2922A= XP_016884848.1:p.Pro974=
XM_017029360.1:c.2454A= XP_016884849.1:p.Pro818=
XR_938365.2:n.3269A=
NM_001111125.3:c.2952A= MANE Select NP_001104595.1:p.Pro984=
NM_015075.2:c.2337A= NP_055890.1:p.Pro779=