Canonical Allele Identifier: CA2429772708

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241470_53241471delinsCT , CM000685.2:g.53241470_53241471delinsCT	GRCh38
NC_000023.10:g.53270652_53270653delinsCT , CM000685.1:g.53270652_53270653delinsCT	GRCh37
NC_000023.9:g.53287377_53287378delinsCT	NCBI36
NG_021296.1:g.84870_84871delinsAG
NG_021296.2:g.84880_84881delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3174+313_3174+314delinsAG	ENSP00000516672.1:n.3174+313_3174+314delinsAG
ENST00000638521.1:c.967+313_967+314delinsAG
ENST00000638869.1:c.476+313_476+314delinsAG
ENST00000639642.1:c.305+313_305+314delinsAG
ENST00000640005.1:c.78+313_78+314delinsAG	ENSP00000491293.1:n.78+313_78+314delinsAG
ENST00000640694.1:c.3015+313_3015+314delinsAG	ENSP00000492403.1:n.3015+313_3015+314delinsAG
ENST00000642864.1:c.3015+313_3015+314delinsAG MANE Select	ENSP00000495726.1:n.3015+313_3015+314delinsAG
ENST00000674510.1:c.3015+313_3015+314delinsAG	ENSP00000502054.1:n.3015+313_3015+314delinsAG
ENST00000674761.1:n.1635_1636delinsAG
ENST00000675719.1:c.2985+313_2985+314delinsAG	ENSP00000501927.1:n.2985+313_2985+314delinsAG
ENST00000375365.2:c.2400+313_2400+314delinsAG	ENSP00000364514.2:n.2400+313_2400+314delinsAG
ENST00000396435.7:c.3015+313_3015+314delinsAG	ENSP00000379712.3:n.3015+313_3015+314delinsAG
NM_001111125.2:c.3015+313_3015+314delinsAG	NP_001104595.1:n.3015+313_3015+314delinsAG
NM_015075.1:c.2400+313_2400+314delinsAG	NP_055890.1:n.2400+313_2400+314delinsAG
XM_006724579.2:c.3111+313_3111+314delinsAG	XP_006724642.1:n.3111+313_3111+314delinsAG
XM_006724580.2:c.2400+313_2400+314delinsAG	XP_006724643.1:n.2400+313_2400+314delinsAG
XM_006724581.2:c.3111+313_3111+314delinsAG	XP_006724644.1:n.3111+313_3111+314delinsAG
XM_006724582.2:c.3111+313_3111+314delinsAG	XP_006724645.1:n.3111+313_3111+314delinsAG
XM_006724583.2:c.3111+313_3111+314delinsAG	XP_006724646.1:n.3111+313_3111+314delinsAG
XM_006724584.2:c.3111+313_3111+314delinsAG	XP_006724647.1:n.3111+313_3111+314delinsAG
XM_011530772.1:c.2337+313_2337+314delinsAG	XP_011529074.1:n.2337+313_2337+314delinsAG
XM_011530773.1:c.2304+313_2304+314delinsAG	XP_011529075.1:n.2304+313_2304+314delinsAG
XM_011530774.1:c.3111+313_3111+314delinsAG	XP_011529076.1:n.3111+313_3111+314delinsAG
XM_011530775.1:c.3111+313_3111+314delinsAG	XP_011529077.1:n.3111+313_3111+314delinsAG
XM_011530776.1:c.3111+313_3111+314delinsAG	XP_011529078.1:n.3111+313_3111+314delinsAG
XM_011530777.1:c.3111+313_3111+314delinsAG	XP_011529079.1:n.3111+313_3111+314delinsAG
XR_938365.1:n.3338+313_3338+314delinsAG
XM_006724579.3:c.3111+313_3111+314delinsAG	XP_006724642.1:n.3111+313_3111+314delinsAG
XM_006724580.3:c.2400+313_2400+314delinsAG	XP_006724643.1:n.2400+313_2400+314delinsAG
XM_006724581.4:c.3111+313_3111+314delinsAG	XP_006724644.1:n.3111+313_3111+314delinsAG
XM_006724582.4:c.3111+313_3111+314delinsAG	XP_006724645.1:n.3111+313_3111+314delinsAG
XM_006724583.4:c.3111+313_3111+314delinsAG	XP_006724646.1:n.3111+313_3111+314delinsAG
XM_006724584.3:c.3111+313_3111+314delinsAG	XP_006724647.1:n.3111+313_3111+314delinsAG
XM_011530773.2:c.2304+313_2304+314delinsAG	XP_011529075.1:n.2304+313_2304+314delinsAG
XM_011530774.3:c.3111+313_3111+314delinsAG	XP_011529076.1:n.3111+313_3111+314delinsAG
XM_011530776.2:c.3111+313_3111+314delinsAG	XP_011529078.1:n.3111+313_3111+314delinsAG
XM_011530777.2:c.3111+313_3111+314delinsAG	XP_011529079.1:n.3111+313_3111+314delinsAG
XM_017029359.2:c.2985+313_2985+314delinsAG	XP_016884848.1:n.2985+313_2985+314delinsAG
XM_017029360.1:c.2517+313_2517+314delinsAG	XP_016884849.1:n.2517+313_2517+314delinsAG
XR_938365.2:n.3332+313_3332+314delinsAG
NM_001111125.3:c.3015+313_3015+314delinsAG MANE Select	NP_001104595.1:n.3015+313_3015+314delinsAG
NM_015075.2:c.2400+313_2400+314delinsAG	NP_055890.1:n.2400+313_2400+314delinsAG