Canonical Allele Identifier: CA413171899
Gene: IQSEC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53255960T>G , CM000685.2:g.53255960T>G GRCh38
NC_000023.10:g.53285142T>G , CM000685.1:g.53285142T>G GRCh37
NC_000023.9:g.53301867T>G NCBI36
NG_021296.1:g.70381A>C
NG_021296.2:g.70391A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.998A>C ENSP00000516672.1:p.His333Pro
ENST00000638630.1:c.128A>C ENSP00000492390.1:p.His43Pro
ENST00000640694.1:c.839A>C ENSP00000492403.1:p.His280Pro
ENST00000642864.1:c.839A>C MANE Select ENSP00000495726.1:p.His280Pro
ENST00000674510.1:c.839A>C ENSP00000502054.1:p.His280Pro
ENST00000675719.1:c.809A>C ENSP00000501927.1:p.His270Pro
ENST00000375365.2:c.224A>C ENSP00000364514.2:p.His75Pro
ENST00000396435.7:c.839A>C ENSP00000379712.3:p.His280Pro
NM_001111125.2:c.839A>C NP_001104595.1:p.His280Pro
NM_015075.1:c.224A>C NP_055890.1:p.His75Pro
XM_006724579.2:c.935A>C XP_006724642.1:p.His312Pro
XM_006724580.2:c.224A>C XP_006724643.1:p.His75Pro
XM_006724581.2:c.935A>C XP_006724644.1:p.His312Pro
XM_006724582.2:c.935A>C XP_006724645.1:p.His312Pro
XM_006724583.2:c.935A>C XP_006724646.1:p.His312Pro
XM_006724584.2:c.935A>C XP_006724647.1:p.His312Pro
XM_011530772.1:c.161A>C XP_011529074.1:p.His54Pro
XM_011530773.1:c.128A>C XP_011529075.1:p.His43Pro
XM_011530774.1:c.935A>C XP_011529076.1:p.His312Pro
XM_011530775.1:c.935A>C XP_011529077.1:p.His312Pro
XM_011530776.1:c.935A>C XP_011529078.1:p.His312Pro
XM_011530777.1:c.935A>C XP_011529079.1:p.His312Pro
XR_938365.1:n.1162A>C
XM_006724579.3:c.935A>C XP_006724642.1:p.His312Pro
XM_006724580.3:c.224A>C XP_006724643.1:p.His75Pro
XM_006724581.4:c.935A>C XP_006724644.1:p.His312Pro
XM_006724582.4:c.935A>C XP_006724645.1:p.His312Pro
XM_006724583.4:c.935A>C XP_006724646.1:p.His312Pro
XM_006724584.3:c.935A>C XP_006724647.1:p.His312Pro
XM_011530773.2:c.128A>C XP_011529075.1:p.His43Pro
XM_011530774.3:c.935A>C XP_011529076.1:p.His312Pro
XM_011530776.2:c.935A>C XP_011529078.1:p.His312Pro
XM_011530777.2:c.935A>C XP_011529079.1:p.His312Pro
XM_017029359.2:c.809A>C XP_016884848.1:p.His270Pro
XM_017029360.1:c.341A>C XP_016884849.1:p.His114Pro
XR_938365.2:n.1156A>C
NM_001111125.3:c.839A>C MANE Select NP_001104595.1:p.His280Pro
NM_015075.2:c.224A>C NP_055890.1:p.His75Pro