Canonical Allele Identifier: CA2429774940

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248254_53248255delinsAG , CM000685.2:g.53248254_53248255delinsAG	GRCh38
NC_000023.10:g.53277436_53277437delinsAG , CM000685.1:g.53277436_53277437delinsAG	GRCh37
NC_000023.9:g.53294161_53294162delinsAG	NCBI36
NG_021296.1:g.78086_78087delinsCT
NG_021296.2:g.78096_78097delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2619-19_2619-18delinsCT	ENSP00000516672.1:n.2619-19_2619-18delinsCT
ENST00000638521.1:c.412-19_412-18delinsCT
ENST00000640694.1:c.2460-19_2460-18delinsCT	ENSP00000492403.1:n.2460-19_2460-18delinsCT
ENST00000642864.1:c.2460-19_2460-18delinsCT MANE Select	ENSP00000495726.1:n.2460-19_2460-18delinsCT
ENST00000674510.1:c.2460-19_2460-18delinsCT	ENSP00000502054.1:n.2460-19_2460-18delinsCT
ENST00000674761.1:n.192_193delinsCT
ENST00000675719.1:c.2430-19_2430-18delinsCT	ENSP00000501927.1:n.2430-19_2430-18delinsCT
ENST00000375365.2:c.1845-19_1845-18delinsCT	ENSP00000364514.2:n.1845-19_1845-18delinsCT
ENST00000396435.7:c.2460-19_2460-18delinsCT	ENSP00000379712.3:n.2460-19_2460-18delinsCT
NM_001111125.2:c.2460-19_2460-18delinsCT	NP_001104595.1:n.2460-19_2460-18delinsCT
NM_015075.1:c.1845-19_1845-18delinsCT	NP_055890.1:n.1845-19_1845-18delinsCT
XM_006724579.2:c.2556-19_2556-18delinsCT	XP_006724642.1:n.2556-19_2556-18delinsCT
XM_006724580.2:c.1845-19_1845-18delinsCT	XP_006724643.1:n.1845-19_1845-18delinsCT
XM_006724581.2:c.2556-19_2556-18delinsCT	XP_006724644.1:n.2556-19_2556-18delinsCT
XM_006724582.2:c.2556-19_2556-18delinsCT	XP_006724645.1:n.2556-19_2556-18delinsCT
XM_006724583.2:c.2556-19_2556-18delinsCT	XP_006724646.1:n.2556-19_2556-18delinsCT
XM_006724584.2:c.2556-19_2556-18delinsCT	XP_006724647.1:n.2556-19_2556-18delinsCT
XM_011530772.1:c.1782-19_1782-18delinsCT	XP_011529074.1:n.1782-19_1782-18delinsCT
XM_011530773.1:c.1749-19_1749-18delinsCT	XP_011529075.1:n.1749-19_1749-18delinsCT
XM_011530774.1:c.2556-19_2556-18delinsCT	XP_011529076.1:n.2556-19_2556-18delinsCT
XM_011530775.1:c.2556-19_2556-18delinsCT	XP_011529077.1:n.2556-19_2556-18delinsCT
XM_011530776.1:c.2556-19_2556-18delinsCT	XP_011529078.1:n.2556-19_2556-18delinsCT
XM_011530777.1:c.2556-19_2556-18delinsCT	XP_011529079.1:n.2556-19_2556-18delinsCT
XR_938365.1:n.2783-19_2783-18delinsCT
XM_006724579.3:c.2556-19_2556-18delinsCT	XP_006724642.1:n.2556-19_2556-18delinsCT
XM_006724580.3:c.1845-19_1845-18delinsCT	XP_006724643.1:n.1845-19_1845-18delinsCT
XM_006724581.4:c.2556-19_2556-18delinsCT	XP_006724644.1:n.2556-19_2556-18delinsCT
XM_006724582.4:c.2556-19_2556-18delinsCT	XP_006724645.1:n.2556-19_2556-18delinsCT
XM_006724583.4:c.2556-19_2556-18delinsCT	XP_006724646.1:n.2556-19_2556-18delinsCT
XM_006724584.3:c.2556-19_2556-18delinsCT	XP_006724647.1:n.2556-19_2556-18delinsCT
XM_011530773.2:c.1749-19_1749-18delinsCT	XP_011529075.1:n.1749-19_1749-18delinsCT
XM_011530774.3:c.2556-19_2556-18delinsCT	XP_011529076.1:n.2556-19_2556-18delinsCT
XM_011530776.2:c.2556-19_2556-18delinsCT	XP_011529078.1:n.2556-19_2556-18delinsCT
XM_011530777.2:c.2556-19_2556-18delinsCT	XP_011529079.1:n.2556-19_2556-18delinsCT
XM_017029359.2:c.2430-19_2430-18delinsCT	XP_016884848.1:n.2430-19_2430-18delinsCT
XM_017029360.1:c.1962-19_1962-18delinsCT	XP_016884849.1:n.1962-19_1962-18delinsCT
XR_938365.2:n.2777-19_2777-18delinsCT
NM_001111125.3:c.2460-19_2460-18delinsCT MANE Select	NP_001104595.1:n.2460-19_2460-18delinsCT
NM_015075.2:c.1845-19_1845-18delinsCT	NP_055890.1:n.1845-19_1845-18delinsCT