Canonical Allele Identifier: CA413172039
Gene: IQSEC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53255985T>G , CM000685.2:g.53255985T>G GRCh38
NC_000023.10:g.53285167T>G , CM000685.1:g.53285167T>G GRCh37
NC_000023.9:g.53301892T>G NCBI36
NG_021296.1:g.70356A>C
NG_021296.2:g.70366A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.973A>C ENSP00000516672.1:p.Ser325Arg
ENST00000638630.1:c.103A>C ENSP00000492390.1:p.Ser35Arg
ENST00000640694.1:c.814A>C ENSP00000492403.1:p.Ser272Arg
ENST00000642864.1:c.814A>C MANE Select ENSP00000495726.1:p.Ser272Arg
ENST00000674510.1:c.814A>C ENSP00000502054.1:p.Ser272Arg
ENST00000675719.1:c.784A>C ENSP00000501927.1:p.Ser262Arg
ENST00000375365.2:c.199A>C ENSP00000364514.2:p.Ser67Arg
ENST00000396435.7:c.814A>C ENSP00000379712.3:p.Ser272Arg
NM_001111125.2:c.814A>C NP_001104595.1:p.Ser272Arg
NM_015075.1:c.199A>C NP_055890.1:p.Ser67Arg
XM_006724579.2:c.910A>C XP_006724642.1:p.Ser304Arg
XM_006724580.2:c.199A>C XP_006724643.1:p.Ser67Arg
XM_006724581.2:c.910A>C XP_006724644.1:p.Ser304Arg
XM_006724582.2:c.910A>C XP_006724645.1:p.Ser304Arg
XM_006724583.2:c.910A>C XP_006724646.1:p.Ser304Arg
XM_006724584.2:c.910A>C XP_006724647.1:p.Ser304Arg
XM_011530772.1:c.136A>C XP_011529074.1:p.Ser46Arg
XM_011530773.1:c.103A>C XP_011529075.1:p.Ser35Arg
XM_011530774.1:c.910A>C XP_011529076.1:p.Ser304Arg
XM_011530775.1:c.910A>C XP_011529077.1:p.Ser304Arg
XM_011530776.1:c.910A>C XP_011529078.1:p.Ser304Arg
XM_011530777.1:c.910A>C XP_011529079.1:p.Ser304Arg
XR_938365.1:n.1137A>C
XM_006724579.3:c.910A>C XP_006724642.1:p.Ser304Arg
XM_006724580.3:c.199A>C XP_006724643.1:p.Ser67Arg
XM_006724581.4:c.910A>C XP_006724644.1:p.Ser304Arg
XM_006724582.4:c.910A>C XP_006724645.1:p.Ser304Arg
XM_006724583.4:c.910A>C XP_006724646.1:p.Ser304Arg
XM_006724584.3:c.910A>C XP_006724647.1:p.Ser304Arg
XM_011530773.2:c.103A>C XP_011529075.1:p.Ser35Arg
XM_011530774.3:c.910A>C XP_011529076.1:p.Ser304Arg
XM_011530776.2:c.910A>C XP_011529078.1:p.Ser304Arg
XM_011530777.2:c.910A>C XP_011529079.1:p.Ser304Arg
XM_017029359.2:c.784A>C XP_016884848.1:p.Ser262Arg
XM_017029360.1:c.316A>C XP_016884849.1:p.Ser106Arg
XR_938365.2:n.1131A>C
NM_001111125.3:c.814A>C MANE Select NP_001104595.1:p.Ser272Arg
NM_015075.2:c.199A>C NP_055890.1:p.Ser67Arg