Canonical Allele Identifier: CA413140797

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53264072C>A (hg19) ; chrX:g.53234890C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53234890C>A , CM000685.2:g.53234890C>A	GRCh38
NC_000023.10:g.53264072C>A , CM000685.1:g.53264072C>A	GRCh37
NC_000023.9:g.53280797C>A	NCBI36
NG_021296.1:g.91451G>T
NG_021296.2:g.91461G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3955G>T	ENSP00000516672.1:p.Ala1319Ser
ENST00000638521.1:c.1453+893G>T
ENST00000638869.1:c.962+893G>T
ENST00000639796.1:c.316+1432G>T	ENSP00000492252.1:n.316+1432G>T
ENST00000640005.1:c.514+1432G>T	ENSP00000491293.1:n.514+1432G>T
ENST00000640694.1:c.*281G>T	ENSP00000492403.1:n.*281G>T
ENST00000642864.1:c.3796G>T MANE Select	ENSP00000495726.1:p.Ala1266Ser
ENST00000674510.1:c.3796G>T	ENSP00000502054.1:p.Ala1266Ser
ENST00000675719.1:c.3766G>T	ENSP00000501927.1:p.Ala1256Ser
ENST00000375365.2:c.*281G>T	ENSP00000364514.2:n.*281G>T
ENST00000396435.7:c.3796G>T	ENSP00000379712.3:p.Ala1266Ser
NM_001111125.2:c.3796G>T	NP_001104595.1:p.Ala1266Ser
NM_015075.1:c.*281G>T	NP_055890.1:n.*281G>T
XM_006724579.2:c.3892G>T	XP_006724642.1:p.Ala1298Ser
XM_006724580.2:c.3181G>T	XP_006724643.1:p.Ala1061Ser
XM_006724581.2:c.3597+893G>T	XP_006724644.1:n.3597+893G>T
XM_006724582.2:c.3597+893G>T	XP_006724645.1:n.3597+893G>T
XM_006724583.2:c.3547+1432G>T	XP_006724646.1:n.3547+1432G>T
XM_006724584.2:c.*281G>T	XP_006724647.1:n.*281G>T
XM_011530772.1:c.3118G>T	XP_011529074.1:p.Ala1040Ser
XM_011530773.1:c.3085G>T	XP_011529075.1:p.Ala1029Ser
XM_011530775.1:c.3547+1432G>T	XP_011529077.1:n.3547+1432G>T
XM_006724579.3:c.3892G>T	XP_006724642.1:p.Ala1298Ser
XM_006724580.3:c.3181G>T	XP_006724643.1:p.Ala1061Ser
XM_006724581.4:c.3597+893G>T	XP_006724644.1:n.3597+893G>T
XM_006724582.4:c.3597+893G>T	XP_006724645.1:n.3597+893G>T
XM_006724583.4:c.3547+1432G>T	XP_006724646.1:n.3547+1432G>T
XM_006724584.3:c.*281G>T	XP_006724647.1:n.*281G>T
XM_011530773.2:c.3085G>T	XP_011529075.1:p.Ala1029Ser
XM_017029359.2:c.3766G>T	XP_016884848.1:p.Ala1256Ser
XM_017029360.1:c.3298G>T	XP_016884849.1:p.Ala1100Ser
NM_001111125.3:c.3796G>T MANE Select	NP_001104595.1:p.Ala1266Ser
NM_015075.2:c.*281G>T	NP_055890.1:n.*281G>T