Canonical Allele Identifier: CA2695233943

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53255949_53255950insC , CM000685.2:g.53255949_53255950insC	GRCh38
NC_000023.10:g.53285131_53285132insC , CM000685.1:g.53285131_53285132insC	GRCh37
NC_000023.9:g.53301856_53301857insC	NCBI36
NG_021296.1:g.70391_70392insG
NG_021296.2:g.70401_70402insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1008_1009insG	ENSP00000516672.1:p.Pro337AlafsTer?
ENST00000638630.1:c.138_139insG	ENSP00000492390.1:p.Pro47AlafsTer?
ENST00000640694.1:c.849_850insG	ENSP00000492403.1:p.Pro284AlafsTer?
ENST00000642864.1:c.849_850insG MANE Select	ENSP00000495726.1:p.Pro284AlafsTer?
ENST00000674510.1:c.849_850insG	ENSP00000502054.1:p.Pro284AlafsTer?
ENST00000675719.1:c.819_820insG	ENSP00000501927.1:p.Pro274AlafsTer?
ENST00000375365.2:c.234_235insG	ENSP00000364514.2:p.Pro79AlafsTer?
ENST00000396435.7:c.849_850insG	ENSP00000379712.3:p.Pro284AlafsTer?
NM_001111125.2:c.849_850insG	NP_001104595.1:p.Pro284AlafsTer?
NM_015075.1:c.234_235insG	NP_055890.1:p.Pro79AlafsTer?
XM_006724579.2:c.945_946insG	XP_006724642.1:p.Pro316AlafsTer?
XM_006724580.2:c.234_235insG	XP_006724643.1:p.Pro79AlafsTer?
XM_006724581.2:c.945_946insG	XP_006724644.1:p.Pro316AlafsTer?
XM_006724582.2:c.945_946insG	XP_006724645.1:p.Pro316AlafsTer?
XM_006724583.2:c.945_946insG	XP_006724646.1:p.Pro316AlafsTer?
XM_006724584.2:c.945_946insG	XP_006724647.1:p.Pro316AlafsTer?
XM_011530772.1:c.171_172insG	XP_011529074.1:p.Pro58AlafsTer?
XM_011530773.1:c.138_139insG	XP_011529075.1:p.Pro47AlafsTer?
XM_011530774.1:c.945_946insG	XP_011529076.1:p.Pro316AlafsTer?
XM_011530775.1:c.945_946insG	XP_011529077.1:p.Pro316AlafsTer?
XM_011530776.1:c.945_946insG	XP_011529078.1:p.Pro316AlafsTer?
XM_011530777.1:c.945_946insG	XP_011529079.1:p.Pro316AlafsTer?
XR_938365.1:n.1172_1173insG
XM_006724579.3:c.945_946insG	XP_006724642.1:p.Pro316AlafsTer?
XM_006724580.3:c.234_235insG	XP_006724643.1:p.Pro79AlafsTer?
XM_006724581.4:c.945_946insG	XP_006724644.1:p.Pro316AlafsTer?
XM_006724582.4:c.945_946insG	XP_006724645.1:p.Pro316AlafsTer?
XM_006724583.4:c.945_946insG	XP_006724646.1:p.Pro316AlafsTer?
XM_006724584.3:c.945_946insG	XP_006724647.1:p.Pro316AlafsTer?
XM_011530773.2:c.138_139insG	XP_011529075.1:p.Pro47AlafsTer?
XM_011530774.3:c.945_946insG	XP_011529076.1:p.Pro316AlafsTer?
XM_011530776.2:c.945_946insG	XP_011529078.1:p.Pro316AlafsTer?
XM_011530777.2:c.945_946insG	XP_011529079.1:p.Pro316AlafsTer?
XM_017029359.2:c.819_820insG	XP_016884848.1:p.Pro274AlafsTer?
XM_017029360.1:c.351_352insG	XP_016884849.1:p.Pro118AlafsTer?
XR_938365.2:n.1166_1167insG
NM_001111125.3:c.849_850insG MANE Select	NP_001104595.1:p.Pro284AlafsTer?
NM_015075.2:c.234_235insG	NP_055890.1:p.Pro79AlafsTer?