Canonical Allele Identifier: CA413171514

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53285073A>G (hg19) ; chrX:g.53255891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53255891A>G , CM000685.2:g.53255891A>G	GRCh38
NC_000023.10:g.53285073A>G , CM000685.1:g.53285073A>G	GRCh37
NC_000023.9:g.53301798A>G	NCBI36
NG_021296.1:g.70450T>C
NG_021296.2:g.70460T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1067T>C	ENSP00000516672.1:p.Val356Ala
ENST00000638630.1:c.197T>C	ENSP00000492390.1:p.Val66Ala
ENST00000640694.1:c.908T>C	ENSP00000492403.1:p.Val303Ala
ENST00000642864.1:c.908T>C MANE Select	ENSP00000495726.1:p.Val303Ala
ENST00000674510.1:c.908T>C	ENSP00000502054.1:p.Val303Ala
ENST00000675719.1:c.878T>C	ENSP00000501927.1:p.Val293Ala
ENST00000375365.2:c.293T>C	ENSP00000364514.2:p.Val98Ala
ENST00000396435.7:c.908T>C	ENSP00000379712.3:p.Val303Ala
NM_001111125.2:c.908T>C	NP_001104595.1:p.Val303Ala
NM_015075.1:c.293T>C	NP_055890.1:p.Val98Ala
XM_006724579.2:c.1004T>C	XP_006724642.1:p.Val335Ala
XM_006724580.2:c.293T>C	XP_006724643.1:p.Val98Ala
XM_006724581.2:c.1004T>C	XP_006724644.1:p.Val335Ala
XM_006724582.2:c.1004T>C	XP_006724645.1:p.Val335Ala
XM_006724583.2:c.1004T>C	XP_006724646.1:p.Val335Ala
XM_006724584.2:c.1004T>C	XP_006724647.1:p.Val335Ala
XM_011530772.1:c.230T>C	XP_011529074.1:p.Val77Ala
XM_011530773.1:c.197T>C	XP_011529075.1:p.Val66Ala
XM_011530774.1:c.1004T>C	XP_011529076.1:p.Val335Ala
XM_011530775.1:c.1004T>C	XP_011529077.1:p.Val335Ala
XM_011530776.1:c.1004T>C	XP_011529078.1:p.Val335Ala
XM_011530777.1:c.1004T>C	XP_011529079.1:p.Val335Ala
XR_938365.1:n.1231T>C
XM_006724579.3:c.1004T>C	XP_006724642.1:p.Val335Ala
XM_006724580.3:c.293T>C	XP_006724643.1:p.Val98Ala
XM_006724581.4:c.1004T>C	XP_006724644.1:p.Val335Ala
XM_006724582.4:c.1004T>C	XP_006724645.1:p.Val335Ala
XM_006724583.4:c.1004T>C	XP_006724646.1:p.Val335Ala
XM_006724584.3:c.1004T>C	XP_006724647.1:p.Val335Ala
XM_011530773.2:c.197T>C	XP_011529075.1:p.Val66Ala
XM_011530774.3:c.1004T>C	XP_011529076.1:p.Val335Ala
XM_011530776.2:c.1004T>C	XP_011529078.1:p.Val335Ala
XM_011530777.2:c.1004T>C	XP_011529079.1:p.Val335Ala
XM_017029359.2:c.878T>C	XP_016884848.1:p.Val293Ala
XM_017029360.1:c.410T>C	XP_016884849.1:p.Val137Ala
XR_938365.2:n.1225T>C
NM_001111125.3:c.908T>C MANE Select	NP_001104595.1:p.Val303Ala
NM_015075.2:c.293T>C	NP_055890.1:p.Val98Ala