Canonical Allele Identifier: CA2429774942

Gene: IQSEC2

Linked Data

• dbSNP Id: rs2074336915

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248257_53248258insA , CM000685.2:g.53248257_53248258insA	GRCh38
NC_000023.10:g.53277439_53277440insA , CM000685.1:g.53277439_53277440insA	GRCh37
NC_000023.9:g.53294164_53294165insA	NCBI36
NG_021296.1:g.78083_78084insT
NG_021296.2:g.78093_78094insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2619-22_2619-21insT	ENSP00000516672.1:n.2619-22_2619-21insT
ENST00000638521.1:c.412-22_412-21insT
ENST00000640694.1:c.2460-22_2460-21insT	ENSP00000492403.1:n.2460-22_2460-21insT
ENST00000642864.1:c.2460-22_2460-21insT MANE Select	ENSP00000495726.1:n.2460-22_2460-21insT
ENST00000674510.1:c.2460-22_2460-21insT	ENSP00000502054.1:n.2460-22_2460-21insT
ENST00000674761.1:n.189_190insT
ENST00000675719.1:c.2430-22_2430-21insT	ENSP00000501927.1:n.2430-22_2430-21insT
ENST00000375365.2:c.1845-22_1845-21insT	ENSP00000364514.2:n.1845-22_1845-21insT
ENST00000396435.7:c.2460-22_2460-21insT	ENSP00000379712.3:n.2460-22_2460-21insT
NM_001111125.2:c.2460-22_2460-21insT	NP_001104595.1:n.2460-22_2460-21insT
NM_015075.1:c.1845-22_1845-21insT	NP_055890.1:n.1845-22_1845-21insT
XM_006724579.2:c.2556-22_2556-21insT	XP_006724642.1:n.2556-22_2556-21insT
XM_006724580.2:c.1845-22_1845-21insT	XP_006724643.1:n.1845-22_1845-21insT
XM_006724581.2:c.2556-22_2556-21insT	XP_006724644.1:n.2556-22_2556-21insT
XM_006724582.2:c.2556-22_2556-21insT	XP_006724645.1:n.2556-22_2556-21insT
XM_006724583.2:c.2556-22_2556-21insT	XP_006724646.1:n.2556-22_2556-21insT
XM_006724584.2:c.2556-22_2556-21insT	XP_006724647.1:n.2556-22_2556-21insT
XM_011530772.1:c.1782-22_1782-21insT	XP_011529074.1:n.1782-22_1782-21insT
XM_011530773.1:c.1749-22_1749-21insT	XP_011529075.1:n.1749-22_1749-21insT
XM_011530774.1:c.2556-22_2556-21insT	XP_011529076.1:n.2556-22_2556-21insT
XM_011530775.1:c.2556-22_2556-21insT	XP_011529077.1:n.2556-22_2556-21insT
XM_011530776.1:c.2556-22_2556-21insT	XP_011529078.1:n.2556-22_2556-21insT
XM_011530777.1:c.2556-22_2556-21insT	XP_011529079.1:n.2556-22_2556-21insT
XR_938365.1:n.2783-22_2783-21insT
XM_006724579.3:c.2556-22_2556-21insT	XP_006724642.1:n.2556-22_2556-21insT
XM_006724580.3:c.1845-22_1845-21insT	XP_006724643.1:n.1845-22_1845-21insT
XM_006724581.4:c.2556-22_2556-21insT	XP_006724644.1:n.2556-22_2556-21insT
XM_006724582.4:c.2556-22_2556-21insT	XP_006724645.1:n.2556-22_2556-21insT
XM_006724583.4:c.2556-22_2556-21insT	XP_006724646.1:n.2556-22_2556-21insT
XM_006724584.3:c.2556-22_2556-21insT	XP_006724647.1:n.2556-22_2556-21insT
XM_011530773.2:c.1749-22_1749-21insT	XP_011529075.1:n.1749-22_1749-21insT
XM_011530774.3:c.2556-22_2556-21insT	XP_011529076.1:n.2556-22_2556-21insT
XM_011530776.2:c.2556-22_2556-21insT	XP_011529078.1:n.2556-22_2556-21insT
XM_011530777.2:c.2556-22_2556-21insT	XP_011529079.1:n.2556-22_2556-21insT
XM_017029359.2:c.2430-22_2430-21insT	XP_016884848.1:n.2430-22_2430-21insT
XM_017029360.1:c.1962-22_1962-21insT	XP_016884849.1:n.1962-22_1962-21insT
XR_938365.2:n.2777-22_2777-21insT
NM_001111125.3:c.2460-22_2460-21insT MANE Select	NP_001104595.1:n.2460-22_2460-21insT
NM_015075.2:c.1845-22_1845-21insT	NP_055890.1:n.1845-22_1845-21insT