Canonical Allele Identifier: CA413140386

Gene: IQSEC2

Linked Data

• gnomAD v4: X-53234823-G-T
• MyVariant Identifiers: chrX:g.53264005G>T (hg19) ; chrX:g.53234823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53234823G>T , CM000685.2:g.53234823G>T	GRCh38
NC_000023.10:g.53264005G>T , CM000685.1:g.53264005G>T	GRCh37
NC_000023.9:g.53280730G>T	NCBI36
NG_021296.1:g.91518C>A
NG_021296.2:g.91528C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.4022C>A	ENSP00000516672.1:p.Pro1341His
ENST00000638521.1:c.1453+960C>A
ENST00000638869.1:c.962+960C>A
ENST00000639796.1:c.316+1499C>A	ENSP00000492252.1:n.316+1499C>A
ENST00000640005.1:c.514+1499C>A	ENSP00000491293.1:n.514+1499C>A
ENST00000640694.1:c.*348C>A	ENSP00000492403.1:n.*348C>A
ENST00000642864.1:c.3863C>A MANE Select	ENSP00000495726.1:p.Pro1288His
ENST00000674510.1:c.3863C>A	ENSP00000502054.1:p.Pro1288His
ENST00000675719.1:c.3833C>A	ENSP00000501927.1:p.Pro1278His
ENST00000375365.2:c.*348C>A	ENSP00000364514.2:n.*348C>A
ENST00000396435.7:c.3863C>A	ENSP00000379712.3:p.Pro1288His
NM_001111125.2:c.3863C>A	NP_001104595.1:p.Pro1288His
NM_015075.1:c.*348C>A	NP_055890.1:n.*348C>A
XM_006724579.2:c.3959C>A	XP_006724642.1:p.Pro1320His
XM_006724580.2:c.3248C>A	XP_006724643.1:p.Pro1083His
XM_006724581.2:c.3597+960C>A	XP_006724644.1:n.3597+960C>A
XM_006724582.2:c.3597+960C>A	XP_006724645.1:n.3597+960C>A
XM_006724583.2:c.3547+1499C>A	XP_006724646.1:n.3547+1499C>A
XM_006724584.2:c.*348C>A	XP_006724647.1:n.*348C>A
XM_011530772.1:c.3185C>A	XP_011529074.1:p.Pro1062His
XM_011530773.1:c.3152C>A	XP_011529075.1:p.Pro1051His
XM_011530775.1:c.3547+1499C>A	XP_011529077.1:n.3547+1499C>A
XM_006724579.3:c.3959C>A	XP_006724642.1:p.Pro1320His
XM_006724580.3:c.3248C>A	XP_006724643.1:p.Pro1083His
XM_006724581.4:c.3597+960C>A	XP_006724644.1:n.3597+960C>A
XM_006724582.4:c.3597+960C>A	XP_006724645.1:n.3597+960C>A
XM_006724583.4:c.3547+1499C>A	XP_006724646.1:n.3547+1499C>A
XM_006724584.3:c.*348C>A	XP_006724647.1:n.*348C>A
XM_011530773.2:c.3152C>A	XP_011529075.1:p.Pro1051His
XM_017029359.2:c.3833C>A	XP_016884848.1:p.Pro1278His
XM_017029360.1:c.3365C>A	XP_016884849.1:p.Pro1122His
NM_001111125.3:c.3863C>A MANE Select	NP_001104595.1:p.Pro1288His
NM_015075.2:c.*348C>A	NP_055890.1:n.*348C>A