Canonical Allele Identifier: CA2429777178
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53255847C= , CM000685.2:g.53255847C= GRCh38
NC_000023.10:g.53285029C= , CM000685.1:g.53285029C= GRCh37
NC_000023.9:g.53301754C= NCBI36
NG_021296.1:g.70494G=
NG_021296.2:g.70504G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.1111G= ENSP00000516672.1:p.Ala371=
ENST00000638630.1:c.241G= ENSP00000492390.1:p.Ala81=
ENST00000640694.1:c.952G= ENSP00000492403.1:p.Ala318=
ENST00000642864.1:c.952G= MANE Select ENSP00000495726.1:p.Ala318=
ENST00000674510.1:c.952G= ENSP00000502054.1:p.Ala318=
ENST00000675719.1:c.922G= ENSP00000501927.1:p.Ala308=
ENST00000375365.2:c.337G= ENSP00000364514.2:p.Ala113=
ENST00000396435.7:c.952G= ENSP00000379712.3:p.Ala318=
NM_001111125.2:c.952G= NP_001104595.1:p.Ala318=
NM_015075.1:c.337G= NP_055890.1:p.Ala113=
XM_006724579.2:c.1048G= XP_006724642.1:p.Ala350=
XM_006724580.2:c.337G= XP_006724643.1:p.Ala113=
XM_006724581.2:c.1048G= XP_006724644.1:p.Ala350=
XM_006724582.2:c.1048G= XP_006724645.1:p.Ala350=
XM_006724583.2:c.1048G= XP_006724646.1:p.Ala350=
XM_006724584.2:c.1048G= XP_006724647.1:p.Ala350=
XM_011530772.1:c.274G= XP_011529074.1:p.Ala92=
XM_011530773.1:c.241G= XP_011529075.1:p.Ala81=
XM_011530774.1:c.1048G= XP_011529076.1:p.Ala350=
XM_011530775.1:c.1048G= XP_011529077.1:p.Ala350=
XM_011530776.1:c.1048G= XP_011529078.1:p.Ala350=
XM_011530777.1:c.1048G= XP_011529079.1:p.Ala350=
XR_938365.1:n.1275G=
XM_006724579.3:c.1048G= XP_006724642.1:p.Ala350=
XM_006724580.3:c.337G= XP_006724643.1:p.Ala113=
XM_006724581.4:c.1048G= XP_006724644.1:p.Ala350=
XM_006724582.4:c.1048G= XP_006724645.1:p.Ala350=
XM_006724583.4:c.1048G= XP_006724646.1:p.Ala350=
XM_006724584.3:c.1048G= XP_006724647.1:p.Ala350=
XM_011530773.2:c.241G= XP_011529075.1:p.Ala81=
XM_011530774.3:c.1048G= XP_011529076.1:p.Ala350=
XM_011530776.2:c.1048G= XP_011529078.1:p.Ala350=
XM_011530777.2:c.1048G= XP_011529079.1:p.Ala350=
XM_017029359.2:c.922G= XP_016884848.1:p.Ala308=
XM_017029360.1:c.454G= XP_016884849.1:p.Ala152=
XR_938365.2:n.1269G=
NM_001111125.3:c.952G= MANE Select NP_001104595.1:p.Ala318=
NM_015075.2:c.337G= NP_055890.1:p.Ala113=