Canonical Allele Identifier: CA2429775614
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53250692G= , CM000685.2:g.53250692G= GRCh38
NC_000023.10:g.53279874G= , CM000685.1:g.53279874G= GRCh37
NC_000023.9:g.53296599G= NCBI36
NG_021296.1:g.75649C=
NG_021296.2:g.75659C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.2043C= ENSP00000516672.1:p.Pro681=
ENST00000640694.1:c.1884C= ENSP00000492403.1:p.Pro628=
ENST00000642864.1:c.1884C= MANE Select ENSP00000495726.1:p.Pro628=
ENST00000674510.1:c.1884C= ENSP00000502054.1:p.Pro628=
ENST00000675719.1:c.1854C= ENSP00000501927.1:p.Pro618=
ENST00000375365.2:c.1269C= ENSP00000364514.2:p.Pro423=
ENST00000396435.7:c.1884C= ENSP00000379712.3:p.Pro628=
NM_001111125.2:c.1884C= NP_001104595.1:p.Pro628=
NM_015075.1:c.1269C= NP_055890.1:p.Pro423=
XM_006724579.2:c.1980C= XP_006724642.1:p.Pro660=
XM_006724580.2:c.1269C= XP_006724643.1:p.Pro423=
XM_006724581.2:c.1980C= XP_006724644.1:p.Pro660=
XM_006724582.2:c.1980C= XP_006724645.1:p.Pro660=
XM_006724583.2:c.1980C= XP_006724646.1:p.Pro660=
XM_006724584.2:c.1980C= XP_006724647.1:p.Pro660=
XM_011530772.1:c.1206C= XP_011529074.1:p.Pro402=
XM_011530773.1:c.1173C= XP_011529075.1:p.Pro391=
XM_011530774.1:c.1980C= XP_011529076.1:p.Pro660=
XM_011530775.1:c.1980C= XP_011529077.1:p.Pro660=
XM_011530776.1:c.1980C= XP_011529078.1:p.Pro660=
XM_011530777.1:c.1980C= XP_011529079.1:p.Pro660=
XR_938365.1:n.2207C=
XM_006724579.3:c.1980C= XP_006724642.1:p.Pro660=
XM_006724580.3:c.1269C= XP_006724643.1:p.Pro423=
XM_006724581.4:c.1980C= XP_006724644.1:p.Pro660=
XM_006724582.4:c.1980C= XP_006724645.1:p.Pro660=
XM_006724583.4:c.1980C= XP_006724646.1:p.Pro660=
XM_006724584.3:c.1980C= XP_006724647.1:p.Pro660=
XM_011530773.2:c.1173C= XP_011529075.1:p.Pro391=
XM_011530774.3:c.1980C= XP_011529076.1:p.Pro660=
XM_011530776.2:c.1980C= XP_011529078.1:p.Pro660=
XM_011530777.2:c.1980C= XP_011529079.1:p.Pro660=
XM_017029359.2:c.1854C= XP_016884848.1:p.Pro618=
XM_017029360.1:c.1386C= XP_016884849.1:p.Pro462=
XR_938365.2:n.2201C=
NM_001111125.3:c.1884C= MANE Select NP_001104595.1:p.Pro628=
NM_015075.2:c.1269C= NP_055890.1:p.Pro423=