Canonical Allele Identifier: CA2693794848

Gene: IQSEC2

Linked Data

• gnomAD v4: X-53235311-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235311A>C , CM000685.2:g.53235311A>C	GRCh38
NC_000023.10:g.53264493A>C , CM000685.1:g.53264493A>C	GRCh37
NC_000023.9:g.53281218A>C	NCBI36
NG_021296.1:g.91030T>G
NG_021296.2:g.91040T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3661-127T>G	ENSP00000516672.1:n.3661-127T>G
ENST00000638521.1:c.1453+472T>G
ENST00000638869.1:c.962+472T>G
ENST00000639796.1:c.316+1011T>G	ENSP00000492252.1:n.316+1011T>G
ENST00000640005.1:c.514+1011T>G	ENSP00000491293.1:n.514+1011T>G
ENST00000640436.1:n.482-127T>G
ENST00000640694.1:c.3452-127T>G	ENSP00000492403.1:n.3452-127T>G
ENST00000642864.1:c.3502-127T>G MANE Select	ENSP00000495726.1:n.3502-127T>G
ENST00000674510.1:c.3502-127T>G	ENSP00000502054.1:n.3502-127T>G
ENST00000675719.1:c.3472-127T>G	ENSP00000501927.1:n.3472-127T>G
ENST00000375365.2:c.2837-127T>G	ENSP00000364514.2:n.2837-127T>G
ENST00000396435.7:c.3502-127T>G	ENSP00000379712.3:n.3502-127T>G
NM_001111125.2:c.3502-127T>G	NP_001104595.1:n.3502-127T>G
NM_015075.1:c.2837-127T>G	NP_055890.1:n.2837-127T>G
XM_006724579.2:c.3598-127T>G	XP_006724642.1:n.3598-127T>G
XM_006724580.2:c.2887-127T>G	XP_006724643.1:n.2887-127T>G
XM_006724581.2:c.3597+472T>G	XP_006724644.1:n.3597+472T>G
XM_006724582.2:c.3597+472T>G	XP_006724645.1:n.3597+472T>G
XM_006724583.2:c.3547+1011T>G	XP_006724646.1:n.3547+1011T>G
XM_006724584.2:c.3548-127T>G	XP_006724647.1:n.3548-127T>G
XM_011530772.1:c.2824-127T>G	XP_011529074.1:n.2824-127T>G
XM_011530773.1:c.2791-127T>G	XP_011529075.1:n.2791-127T>G
XM_011530774.1:c.*176T>G	XP_011529076.1:n.*176T>G
XM_011530775.1:c.3547+1011T>G	XP_011529077.1:n.3547+1011T>G
XM_006724579.3:c.3598-127T>G	XP_006724642.1:n.3598-127T>G
XM_006724580.3:c.2887-127T>G	XP_006724643.1:n.2887-127T>G
XM_006724581.4:c.3597+472T>G	XP_006724644.1:n.3597+472T>G
XM_006724582.4:c.3597+472T>G	XP_006724645.1:n.3597+472T>G
XM_006724583.4:c.3547+1011T>G	XP_006724646.1:n.3547+1011T>G
XM_006724584.3:c.3548-127T>G	XP_006724647.1:n.3548-127T>G
XM_011530773.2:c.2791-127T>G	XP_011529075.1:n.2791-127T>G
XM_011530774.3:c.*176T>G	XP_011529076.1:n.*176T>G
XM_017029359.2:c.3472-127T>G	XP_016884848.1:n.3472-127T>G
XM_017029360.1:c.3004-127T>G	XP_016884849.1:n.3004-127T>G
NM_001111125.3:c.3502-127T>G MANE Select	NP_001104595.1:n.3502-127T>G
NM_015075.2:c.2837-127T>G	NP_055890.1:n.2837-127T>G