Canonical Allele Identifier: CA2499499904

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248139_53248140insG , CM000685.2:g.53248139_53248140insG	GRCh38
NC_000023.10:g.53277321_53277322insG , CM000685.1:g.53277321_53277322insG	GRCh37
NC_000023.9:g.53294046_53294047insG	NCBI36
NG_021296.1:g.78201_78202insC
NG_021296.2:g.78211_78212insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2715_2716insC	ENSP00000516672.1:p.Val906ArgfsTer16
ENST00000638521.1:c.508_509insC
ENST00000638869.1:c.17_18insC
ENST00000640694.1:c.2556_2557insC	ENSP00000492403.1:p.Val853ArgfsTer16
ENST00000642864.1:c.2556_2557insC MANE Select	ENSP00000495726.1:p.Val853ArgfsTer16
ENST00000674510.1:c.2556_2557insC	ENSP00000502054.1:p.Val853ArgfsTer16
ENST00000674761.1:n.307_308insC
ENST00000675719.1:c.2526_2527insC	ENSP00000501927.1:p.Val843ArgfsTer16
ENST00000375365.2:c.1941_1942insC	ENSP00000364514.2:p.Val648ArgfsTer16
ENST00000396435.7:c.2556_2557insC	ENSP00000379712.3:p.Val853ArgfsTer16
NM_001111125.2:c.2556_2557insC	NP_001104595.1:p.Val853ArgfsTer16
NM_015075.1:c.1941_1942insC	NP_055890.1:p.Val648ArgfsTer16
XM_006724579.2:c.2652_2653insC	XP_006724642.1:p.Val885ArgfsTer16
XM_006724580.2:c.1941_1942insC	XP_006724643.1:p.Val648ArgfsTer16
XM_006724581.2:c.2652_2653insC	XP_006724644.1:p.Val885ArgfsTer16
XM_006724582.2:c.2652_2653insC	XP_006724645.1:p.Val885ArgfsTer16
XM_006724583.2:c.2652_2653insC	XP_006724646.1:p.Val885ArgfsTer16
XM_006724584.2:c.2652_2653insC	XP_006724647.1:p.Val885ArgfsTer16
XM_011530772.1:c.1878_1879insC	XP_011529074.1:p.Val627ArgfsTer16
XM_011530773.1:c.1845_1846insC	XP_011529075.1:p.Val616ArgfsTer16
XM_011530774.1:c.2652_2653insC	XP_011529076.1:p.Val885ArgfsTer16
XM_011530775.1:c.2652_2653insC	XP_011529077.1:p.Val885ArgfsTer16
XM_011530776.1:c.2652_2653insC	XP_011529078.1:p.Val885ArgfsTer16
XM_011530777.1:c.2652_2653insC	XP_011529079.1:p.Val885ArgfsTer16
XR_938365.1:n.2879_2880insC
XM_006724579.3:c.2652_2653insC	XP_006724642.1:p.Val885ArgfsTer16
XM_006724580.3:c.1941_1942insC	XP_006724643.1:p.Val648ArgfsTer16
XM_006724581.4:c.2652_2653insC	XP_006724644.1:p.Val885ArgfsTer16
XM_006724582.4:c.2652_2653insC	XP_006724645.1:p.Val885ArgfsTer16
XM_006724583.4:c.2652_2653insC	XP_006724646.1:p.Val885ArgfsTer16
XM_006724584.3:c.2652_2653insC	XP_006724647.1:p.Val885ArgfsTer16
XM_011530773.2:c.1845_1846insC	XP_011529075.1:p.Val616ArgfsTer16
XM_011530774.3:c.2652_2653insC	XP_011529076.1:p.Val885ArgfsTer16
XM_011530776.2:c.2652_2653insC	XP_011529078.1:p.Val885ArgfsTer16
XM_011530777.2:c.2652_2653insC	XP_011529079.1:p.Val885ArgfsTer16
XM_017029359.2:c.2526_2527insC	XP_016884848.1:p.Val843ArgfsTer16
XM_017029360.1:c.2058_2059insC	XP_016884849.1:p.Val687ArgfsTer16
XR_938365.2:n.2873_2874insC
NM_001111125.3:c.2556_2557insC MANE Select	NP_001104595.1:p.Val853ArgfsTer16
NM_015075.2:c.1941_1942insC	NP_055890.1:p.Val648ArgfsTer16