Canonical Allele Identifier: CA2429777229
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53256023G= , CM000685.2:g.53256023G= GRCh38
NC_000023.10:g.53285205G= , CM000685.1:g.53285205G= GRCh37
NC_000023.9:g.53301930G= NCBI36
NG_021296.1:g.70318C=
NG_021296.2:g.70328C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.935C= ENSP00000516672.1:p.Ala312=
ENST00000638630.1:c.65C= ENSP00000492390.1:p.Ala22=
ENST00000640694.1:c.776C= ENSP00000492403.1:p.Ala259=
ENST00000642864.1:c.776C= MANE Select ENSP00000495726.1:p.Ala259=
ENST00000674510.1:c.776C= ENSP00000502054.1:p.Ala259=
ENST00000675719.1:c.746C= ENSP00000501927.1:p.Ala249=
ENST00000375365.2:c.161C= ENSP00000364514.2:p.Ala54=
ENST00000396435.7:c.776C= ENSP00000379712.3:p.Ala259=
NM_001111125.2:c.776C= NP_001104595.1:p.Ala259=
NM_015075.1:c.161C= NP_055890.1:p.Ala54=
XM_006724579.2:c.872C= XP_006724642.1:p.Ala291=
XM_006724580.2:c.161C= XP_006724643.1:p.Ala54=
XM_006724581.2:c.872C= XP_006724644.1:p.Ala291=
XM_006724582.2:c.872C= XP_006724645.1:p.Ala291=
XM_006724583.2:c.872C= XP_006724646.1:p.Ala291=
XM_006724584.2:c.872C= XP_006724647.1:p.Ala291=
XM_011530772.1:c.98C= XP_011529074.1:p.Ala33=
XM_011530773.1:c.65C= XP_011529075.1:p.Ala22=
XM_011530774.1:c.872C= XP_011529076.1:p.Ala291=
XM_011530775.1:c.872C= XP_011529077.1:p.Ala291=
XM_011530776.1:c.872C= XP_011529078.1:p.Ala291=
XM_011530777.1:c.872C= XP_011529079.1:p.Ala291=
XR_938365.1:n.1099C=
XM_006724579.3:c.872C= XP_006724642.1:p.Ala291=
XM_006724580.3:c.161C= XP_006724643.1:p.Ala54=
XM_006724581.4:c.872C= XP_006724644.1:p.Ala291=
XM_006724582.4:c.872C= XP_006724645.1:p.Ala291=
XM_006724583.4:c.872C= XP_006724646.1:p.Ala291=
XM_006724584.3:c.872C= XP_006724647.1:p.Ala291=
XM_011530773.2:c.65C= XP_011529075.1:p.Ala22=
XM_011530774.3:c.872C= XP_011529076.1:p.Ala291=
XM_011530776.2:c.872C= XP_011529078.1:p.Ala291=
XM_011530777.2:c.872C= XP_011529079.1:p.Ala291=
XM_017029359.2:c.746C= XP_016884848.1:p.Ala249=
XM_017029360.1:c.278C= XP_016884849.1:p.Ala93=
XR_938365.2:n.1093C=
NM_001111125.3:c.776C= MANE Select NP_001104595.1:p.Ala259=
NM_015075.2:c.161C= NP_055890.1:p.Ala54=