Canonical Allele Identifier: CA413140700

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53264057A>G (hg19) ; chrX:g.53234875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53234875A>G , CM000685.2:g.53234875A>G	GRCh38
NC_000023.10:g.53264057A>G , CM000685.1:g.53264057A>G	GRCh37
NC_000023.9:g.53280782A>G	NCBI36
NG_021296.1:g.91466T>C
NG_021296.2:g.91476T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3970T>C	ENSP00000516672.1:p.Tyr1324His
ENST00000638521.1:c.1453+908T>C
ENST00000638869.1:c.962+908T>C
ENST00000639796.1:c.316+1447T>C	ENSP00000492252.1:n.316+1447T>C
ENST00000640005.1:c.514+1447T>C	ENSP00000491293.1:n.514+1447T>C
ENST00000640694.1:c.*296T>C	ENSP00000492403.1:n.*296T>C
ENST00000642864.1:c.3811T>C MANE Select	ENSP00000495726.1:p.Tyr1271His
ENST00000674510.1:c.3811T>C	ENSP00000502054.1:p.Tyr1271His
ENST00000675719.1:c.3781T>C	ENSP00000501927.1:p.Tyr1261His
ENST00000375365.2:c.*296T>C	ENSP00000364514.2:n.*296T>C
ENST00000396435.7:c.3811T>C	ENSP00000379712.3:p.Tyr1271His
NM_001111125.2:c.3811T>C	NP_001104595.1:p.Tyr1271His
NM_015075.1:c.*296T>C	NP_055890.1:n.*296T>C
XM_006724579.2:c.3907T>C	XP_006724642.1:p.Tyr1303His
XM_006724580.2:c.3196T>C	XP_006724643.1:p.Tyr1066His
XM_006724581.2:c.3597+908T>C	XP_006724644.1:n.3597+908T>C
XM_006724582.2:c.3597+908T>C	XP_006724645.1:n.3597+908T>C
XM_006724583.2:c.3547+1447T>C	XP_006724646.1:n.3547+1447T>C
XM_006724584.2:c.*296T>C	XP_006724647.1:n.*296T>C
XM_011530772.1:c.3133T>C	XP_011529074.1:p.Tyr1045His
XM_011530773.1:c.3100T>C	XP_011529075.1:p.Tyr1034His
XM_011530775.1:c.3547+1447T>C	XP_011529077.1:n.3547+1447T>C
XM_006724579.3:c.3907T>C	XP_006724642.1:p.Tyr1303His
XM_006724580.3:c.3196T>C	XP_006724643.1:p.Tyr1066His
XM_006724581.4:c.3597+908T>C	XP_006724644.1:n.3597+908T>C
XM_006724582.4:c.3597+908T>C	XP_006724645.1:n.3597+908T>C
XM_006724583.4:c.3547+1447T>C	XP_006724646.1:n.3547+1447T>C
XM_006724584.3:c.*296T>C	XP_006724647.1:n.*296T>C
XM_011530773.2:c.3100T>C	XP_011529075.1:p.Tyr1034His
XM_017029359.2:c.3781T>C	XP_016884848.1:p.Tyr1261His
XM_017029360.1:c.3313T>C	XP_016884849.1:p.Tyr1105His
NM_001111125.3:c.3811T>C MANE Select	NP_001104595.1:p.Tyr1271His
NM_015075.2:c.*296T>C	NP_055890.1:n.*296T>C