Canonical Allele Identifier: CA413149240

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53271024C>G (hg19) ; chrX:g.53241842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241842C>G , CM000685.2:g.53241842C>G	GRCh38
NC_000023.10:g.53271024C>G , CM000685.1:g.53271024C>G	GRCh37
NC_000023.9:g.53287749C>G	NCBI36
NG_021296.1:g.84499G>C
NG_021296.2:g.84509G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3116G>C	ENSP00000516672.1:p.Arg1039Pro
ENST00000638521.1:c.909G>C
ENST00000638869.1:c.418G>C
ENST00000639642.1:c.247G>C
ENST00000640005.1:c.20G>C	ENSP00000491293.1:p.Arg7Pro
ENST00000640694.1:c.2957G>C	ENSP00000492403.1:p.Arg986Pro
ENST00000642864.1:c.2957G>C MANE Select	ENSP00000495726.1:p.Arg986Pro
ENST00000674510.1:c.2957G>C	ENSP00000502054.1:p.Arg986Pro
ENST00000674761.1:n.1264G>C
ENST00000675719.1:c.2927G>C	ENSP00000501927.1:p.Arg976Pro
ENST00000375365.2:c.2342G>C	ENSP00000364514.2:p.Arg781Pro
ENST00000396435.7:c.2957G>C	ENSP00000379712.3:p.Arg986Pro
NM_001111125.2:c.2957G>C	NP_001104595.1:p.Arg986Pro
NM_015075.1:c.2342G>C	NP_055890.1:p.Arg781Pro
XM_006724579.2:c.3053G>C	XP_006724642.1:p.Arg1018Pro
XM_006724580.2:c.2342G>C	XP_006724643.1:p.Arg781Pro
XM_006724581.2:c.3053G>C	XP_006724644.1:p.Arg1018Pro
XM_006724582.2:c.3053G>C	XP_006724645.1:p.Arg1018Pro
XM_006724583.2:c.3053G>C	XP_006724646.1:p.Arg1018Pro
XM_006724584.2:c.3053G>C	XP_006724647.1:p.Arg1018Pro
XM_011530772.1:c.2279G>C	XP_011529074.1:p.Arg760Pro
XM_011530773.1:c.2246G>C	XP_011529075.1:p.Arg749Pro
XM_011530774.1:c.3053G>C	XP_011529076.1:p.Arg1018Pro
XM_011530775.1:c.3053G>C	XP_011529077.1:p.Arg1018Pro
XM_011530776.1:c.3053G>C	XP_011529078.1:p.Arg1018Pro
XM_011530777.1:c.3053G>C	XP_011529079.1:p.Arg1018Pro
XR_938365.1:n.3280G>C
XM_006724579.3:c.3053G>C	XP_006724642.1:p.Arg1018Pro
XM_006724580.3:c.2342G>C	XP_006724643.1:p.Arg781Pro
XM_006724581.4:c.3053G>C	XP_006724644.1:p.Arg1018Pro
XM_006724582.4:c.3053G>C	XP_006724645.1:p.Arg1018Pro
XM_006724583.4:c.3053G>C	XP_006724646.1:p.Arg1018Pro
XM_006724584.3:c.3053G>C	XP_006724647.1:p.Arg1018Pro
XM_011530773.2:c.2246G>C	XP_011529075.1:p.Arg749Pro
XM_011530774.3:c.3053G>C	XP_011529076.1:p.Arg1018Pro
XM_011530776.2:c.3053G>C	XP_011529078.1:p.Arg1018Pro
XM_011530777.2:c.3053G>C	XP_011529079.1:p.Arg1018Pro
XM_017029359.2:c.2927G>C	XP_016884848.1:p.Arg976Pro
XM_017029360.1:c.2459G>C	XP_016884849.1:p.Arg820Pro
XR_938365.2:n.3274G>C
NM_001111125.3:c.2957G>C MANE Select	NP_001104595.1:p.Arg986Pro
NM_015075.2:c.2342G>C	NP_055890.1:p.Arg781Pro