Canonical Allele Identifier: CA2693789525

Gene: IQSEC2

Linked Data

• gnomAD v4: X-53248246-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248250_53248252del , CM000685.2:g.53248250_53248252del	GRCh38
NC_000023.10:g.53277432_53277434del , CM000685.1:g.53277432_53277434del	GRCh37
NC_000023.9:g.53294157_53294159del	NCBI36
NG_021296.1:g.78092_78094del
NG_021296.2:g.78102_78104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2619-13_2619-11del	ENSP00000516672.1:n.2619-13_2619-11del
ENST00000638521.1:c.412-13_412-11del
ENST00000640694.1:c.2460-13_2460-11del	ENSP00000492403.1:n.2460-13_2460-11del
ENST00000642864.1:c.2460-13_2460-11del MANE Select	ENSP00000495726.1:n.2460-13_2460-11del
ENST00000674510.1:c.2460-13_2460-11del	ENSP00000502054.1:n.2460-13_2460-11del
ENST00000674761.1:n.198_200del
ENST00000675719.1:c.2430-13_2430-11del	ENSP00000501927.1:n.2430-13_2430-11del
ENST00000375365.2:c.1845-13_1845-11del	ENSP00000364514.2:n.1845-13_1845-11del
ENST00000396435.7:c.2460-13_2460-11del	ENSP00000379712.3:n.2460-13_2460-11del
NM_001111125.2:c.2460-13_2460-11del	NP_001104595.1:n.2460-13_2460-11del
NM_015075.1:c.1845-13_1845-11del	NP_055890.1:n.1845-13_1845-11del
XM_006724579.2:c.2556-13_2556-11del	XP_006724642.1:n.2556-13_2556-11del
XM_006724580.2:c.1845-13_1845-11del	XP_006724643.1:n.1845-13_1845-11del
XM_006724581.2:c.2556-13_2556-11del	XP_006724644.1:n.2556-13_2556-11del
XM_006724582.2:c.2556-13_2556-11del	XP_006724645.1:n.2556-13_2556-11del
XM_006724583.2:c.2556-13_2556-11del	XP_006724646.1:n.2556-13_2556-11del
XM_006724584.2:c.2556-13_2556-11del	XP_006724647.1:n.2556-13_2556-11del
XM_011530772.1:c.1782-13_1782-11del	XP_011529074.1:n.1782-13_1782-11del
XM_011530773.1:c.1749-13_1749-11del	XP_011529075.1:n.1749-13_1749-11del
XM_011530774.1:c.2556-13_2556-11del	XP_011529076.1:n.2556-13_2556-11del
XM_011530775.1:c.2556-13_2556-11del	XP_011529077.1:n.2556-13_2556-11del
XM_011530776.1:c.2556-13_2556-11del	XP_011529078.1:n.2556-13_2556-11del
XM_011530777.1:c.2556-13_2556-11del	XP_011529079.1:n.2556-13_2556-11del
XR_938365.1:n.2783-13_2783-11del
XM_006724579.3:c.2556-13_2556-11del	XP_006724642.1:n.2556-13_2556-11del
XM_006724580.3:c.1845-13_1845-11del	XP_006724643.1:n.1845-13_1845-11del
XM_006724581.4:c.2556-13_2556-11del	XP_006724644.1:n.2556-13_2556-11del
XM_006724582.4:c.2556-13_2556-11del	XP_006724645.1:n.2556-13_2556-11del
XM_006724583.4:c.2556-13_2556-11del	XP_006724646.1:n.2556-13_2556-11del
XM_006724584.3:c.2556-13_2556-11del	XP_006724647.1:n.2556-13_2556-11del
XM_011530773.2:c.1749-13_1749-11del	XP_011529075.1:n.1749-13_1749-11del
XM_011530774.3:c.2556-13_2556-11del	XP_011529076.1:n.2556-13_2556-11del
XM_011530776.2:c.2556-13_2556-11del	XP_011529078.1:n.2556-13_2556-11del
XM_011530777.2:c.2556-13_2556-11del	XP_011529079.1:n.2556-13_2556-11del
XM_017029359.2:c.2430-13_2430-11del	XP_016884848.1:n.2430-13_2430-11del
XM_017029360.1:c.1962-13_1962-11del	XP_016884849.1:n.1962-13_1962-11del
XR_938365.2:n.2777-13_2777-11del
NM_001111125.3:c.2460-13_2460-11del MANE Select	NP_001104595.1:n.2460-13_2460-11del
NM_015075.2:c.1845-13_1845-11del	NP_055890.1:n.1845-13_1845-11del