Canonical Allele Identifier: CA413157113

Gene: IQSEC2

Linked Data

• ClinVar Variation Id: 982678
• ClinVar RCV Id: RCV001262289
• dbSNP Id: rs2074335877
• MyVariant Identifiers: chrX:g.53277359A>G (hg19) ; chrX:g.53248177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248177A>G , CM000685.2:g.53248177A>G	GRCh38
NC_000023.10:g.53277359A>G , CM000685.1:g.53277359A>G	GRCh37
NC_000023.9:g.53294084A>G	NCBI36
NG_021296.1:g.78164T>C
NG_021296.2:g.78174T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2678T>C	ENSP00000516672.1:p.Phe893Ser
ENST00000638521.1:c.471T>C
ENST00000640694.1:c.2519T>C	ENSP00000492403.1:p.Phe840Ser
ENST00000642864.1:c.2519T>C MANE Select	ENSP00000495726.1:p.Phe840Ser
ENST00000674510.1:c.2519T>C	ENSP00000502054.1:p.Phe840Ser
ENST00000674761.1:n.270T>C
ENST00000675719.1:c.2489T>C	ENSP00000501927.1:p.Phe830Ser
ENST00000375365.2:c.1904T>C	ENSP00000364514.2:p.Phe635Ser
ENST00000396435.7:c.2519T>C	ENSP00000379712.3:p.Phe840Ser
NM_001111125.2:c.2519T>C	NP_001104595.1:p.Phe840Ser
NM_015075.1:c.1904T>C	NP_055890.1:p.Phe635Ser
XM_006724579.2:c.2615T>C	XP_006724642.1:p.Phe872Ser
XM_006724580.2:c.1904T>C	XP_006724643.1:p.Phe635Ser
XM_006724581.2:c.2615T>C	XP_006724644.1:p.Phe872Ser
XM_006724582.2:c.2615T>C	XP_006724645.1:p.Phe872Ser
XM_006724583.2:c.2615T>C	XP_006724646.1:p.Phe872Ser
XM_006724584.2:c.2615T>C	XP_006724647.1:p.Phe872Ser
XM_011530772.1:c.1841T>C	XP_011529074.1:p.Phe614Ser
XM_011530773.1:c.1808T>C	XP_011529075.1:p.Phe603Ser
XM_011530774.1:c.2615T>C	XP_011529076.1:p.Phe872Ser
XM_011530775.1:c.2615T>C	XP_011529077.1:p.Phe872Ser
XM_011530776.1:c.2615T>C	XP_011529078.1:p.Phe872Ser
XM_011530777.1:c.2615T>C	XP_011529079.1:p.Phe872Ser
XR_938365.1:n.2842T>C
XM_006724579.3:c.2615T>C	XP_006724642.1:p.Phe872Ser
XM_006724580.3:c.1904T>C	XP_006724643.1:p.Phe635Ser
XM_006724581.4:c.2615T>C	XP_006724644.1:p.Phe872Ser
XM_006724582.4:c.2615T>C	XP_006724645.1:p.Phe872Ser
XM_006724583.4:c.2615T>C	XP_006724646.1:p.Phe872Ser
XM_006724584.3:c.2615T>C	XP_006724647.1:p.Phe872Ser
XM_011530773.2:c.1808T>C	XP_011529075.1:p.Phe603Ser
XM_011530774.3:c.2615T>C	XP_011529076.1:p.Phe872Ser
XM_011530776.2:c.2615T>C	XP_011529078.1:p.Phe872Ser
XM_011530777.2:c.2615T>C	XP_011529079.1:p.Phe872Ser
XM_017029359.2:c.2489T>C	XP_016884848.1:p.Phe830Ser
XM_017029360.1:c.2021T>C	XP_016884849.1:p.Phe674Ser
XR_938365.2:n.2836T>C
NM_001111125.3:c.2519T>C MANE Select	NP_001104595.1:p.Phe840Ser
NM_015075.2:c.1904T>C	NP_055890.1:p.Phe635Ser