Canonical Allele Identifier: CA413163265
Gene: IQSEC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53250732A>T , CM000685.2:g.53250732A>T GRCh38
NC_000023.10:g.53279914A>T , CM000685.1:g.53279914A>T GRCh37
NC_000023.9:g.53296639A>T NCBI36
NG_021296.1:g.75609T>A
NG_021296.2:g.75619T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.2003T>A ENSP00000516672.1:p.Val668Asp
ENST00000640694.1:c.1844T>A ENSP00000492403.1:p.Val615Asp
ENST00000642864.1:c.1844T>A MANE Select ENSP00000495726.1:p.Val615Asp
ENST00000674510.1:c.1844T>A ENSP00000502054.1:p.Val615Asp
ENST00000675719.1:c.1814T>A ENSP00000501927.1:p.Val605Asp
ENST00000375365.2:c.1229T>A ENSP00000364514.2:p.Val410Asp
ENST00000396435.7:c.1844T>A ENSP00000379712.3:p.Val615Asp
NM_001111125.2:c.1844T>A NP_001104595.1:p.Val615Asp
NM_015075.1:c.1229T>A NP_055890.1:p.Val410Asp
XM_006724579.2:c.1940T>A XP_006724642.1:p.Val647Asp
XM_006724580.2:c.1229T>A XP_006724643.1:p.Val410Asp
XM_006724581.2:c.1940T>A XP_006724644.1:p.Val647Asp
XM_006724582.2:c.1940T>A XP_006724645.1:p.Val647Asp
XM_006724583.2:c.1940T>A XP_006724646.1:p.Val647Asp
XM_006724584.2:c.1940T>A XP_006724647.1:p.Val647Asp
XM_011530772.1:c.1166T>A XP_011529074.1:p.Val389Asp
XM_011530773.1:c.1133T>A XP_011529075.1:p.Val378Asp
XM_011530774.1:c.1940T>A XP_011529076.1:p.Val647Asp
XM_011530775.1:c.1940T>A XP_011529077.1:p.Val647Asp
XM_011530776.1:c.1940T>A XP_011529078.1:p.Val647Asp
XM_011530777.1:c.1940T>A XP_011529079.1:p.Val647Asp
XR_938365.1:n.2167T>A
XM_006724579.3:c.1940T>A XP_006724642.1:p.Val647Asp
XM_006724580.3:c.1229T>A XP_006724643.1:p.Val410Asp
XM_006724581.4:c.1940T>A XP_006724644.1:p.Val647Asp
XM_006724582.4:c.1940T>A XP_006724645.1:p.Val647Asp
XM_006724583.4:c.1940T>A XP_006724646.1:p.Val647Asp
XM_006724584.3:c.1940T>A XP_006724647.1:p.Val647Asp
XM_011530773.2:c.1133T>A XP_011529075.1:p.Val378Asp
XM_011530774.3:c.1940T>A XP_011529076.1:p.Val647Asp
XM_011530776.2:c.1940T>A XP_011529078.1:p.Val647Asp
XM_011530777.2:c.1940T>A XP_011529079.1:p.Val647Asp
XM_017029359.2:c.1814T>A XP_016884848.1:p.Val605Asp
XM_017029360.1:c.1346T>A XP_016884849.1:p.Val449Asp
XR_938365.2:n.2161T>A
NM_001111125.3:c.1844T>A MANE Select NP_001104595.1:p.Val615Asp
NM_015075.2:c.1229T>A NP_055890.1:p.Val410Asp