Canonical Allele Identifier: CA516673897

Gene: IQSEC2

Linked Data

• ClinVar Variation Id: 1733326
• ClinVar RCV Id: RCV002452303
• gnomAD v4: X-53235065-G-A
• MyVariant Identifiers: chrX:g.53264247G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235065G>A , CM000685.2:g.53235065G>A	GRCh38
NC_000023.10:g.53264247G>A , CM000685.1:g.53264247G>A	GRCh37
NC_000023.9:g.53280972G>A	NCBI36
NG_021296.1:g.91276C>T
NG_021296.2:g.91286C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3780C>T	ENSP00000516672.1:p.Ser1260=
ENST00000638521.1:c.1453+718C>T
ENST00000638869.1:c.962+718C>T
ENST00000639796.1:c.316+1257C>T	ENSP00000492252.1:n.316+1257C>T
ENST00000640005.1:c.514+1257C>T	ENSP00000491293.1:n.514+1257C>T
ENST00000640694.1:c.*106C>T	ENSP00000492403.1:n.*106C>T
ENST00000642864.1:c.3621C>T MANE Select	ENSP00000495726.1:p.Ser1207=
ENST00000674510.1:c.3621C>T	ENSP00000502054.1:p.Ser1207=
ENST00000675719.1:c.3591C>T	ENSP00000501927.1:p.Ser1197=
ENST00000375365.2:c.*106C>T	ENSP00000364514.2:n.*106C>T
ENST00000396435.7:c.3621C>T	ENSP00000379712.3:p.Ser1207=
NM_001111125.2:c.3621C>T	NP_001104595.1:p.Ser1207=
NM_015075.1:c.*106C>T	NP_055890.1:n.*106C>T
XM_006724579.2:c.3717C>T	XP_006724642.1:p.Ser1239=
XM_006724580.2:c.3006C>T	XP_006724643.1:p.Ser1002=
XM_006724581.2:c.3597+718C>T	XP_006724644.1:n.3597+718C>T
XM_006724582.2:c.3597+718C>T	XP_006724645.1:n.3597+718C>T
XM_006724583.2:c.3547+1257C>T	XP_006724646.1:n.3547+1257C>T
XM_006724584.2:c.*106C>T	XP_006724647.1:n.*106C>T
XM_011530772.1:c.2943C>T	XP_011529074.1:p.Ser981=
XM_011530773.1:c.2910C>T	XP_011529075.1:p.Ser970=
XM_011530775.1:c.3547+1257C>T	XP_011529077.1:n.3547+1257C>T
XM_006724579.3:c.3717C>T	XP_006724642.1:p.Ser1239=
XM_006724580.3:c.3006C>T	XP_006724643.1:p.Ser1002=
XM_006724581.4:c.3597+718C>T	XP_006724644.1:n.3597+718C>T
XM_006724582.4:c.3597+718C>T	XP_006724645.1:n.3597+718C>T
XM_006724583.4:c.3547+1257C>T	XP_006724646.1:n.3547+1257C>T
XM_006724584.3:c.*106C>T	XP_006724647.1:n.*106C>T
XM_011530773.2:c.2910C>T	XP_011529075.1:p.Ser970=
XM_017029359.2:c.3591C>T	XP_016884848.1:p.Ser1197=
XM_017029360.1:c.3123C>T	XP_016884849.1:p.Ser1041=
NM_001111125.3:c.3621C>T MANE Select	NP_001104595.1:p.Ser1207=
NM_015075.2:c.*106C>T	NP_055890.1:n.*106C>T