Canonical Allele Identifier: CA413163487

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53279947A>G (hg19) ; chrX:g.53250765A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250765A>G , CM000685.2:g.53250765A>G	GRCh38
NC_000023.10:g.53279947A>G , CM000685.1:g.53279947A>G	GRCh37
NC_000023.9:g.53296672A>G	NCBI36
NG_021296.1:g.75576T>C
NG_021296.2:g.75586T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.1970T>C	ENSP00000516672.1:p.Val657Ala
ENST00000640694.1:c.1811T>C	ENSP00000492403.1:p.Val604Ala
ENST00000642864.1:c.1811T>C MANE Select	ENSP00000495726.1:p.Val604Ala
ENST00000674510.1:c.1811T>C	ENSP00000502054.1:p.Val604Ala
ENST00000675719.1:c.1781T>C	ENSP00000501927.1:p.Val594Ala
ENST00000375365.2:c.1196T>C	ENSP00000364514.2:p.Val399Ala
ENST00000396435.7:c.1811T>C	ENSP00000379712.3:p.Val604Ala
NM_001111125.2:c.1811T>C	NP_001104595.1:p.Val604Ala
NM_015075.1:c.1196T>C	NP_055890.1:p.Val399Ala
XM_006724579.2:c.1907T>C	XP_006724642.1:p.Val636Ala
XM_006724580.2:c.1196T>C	XP_006724643.1:p.Val399Ala
XM_006724581.2:c.1907T>C	XP_006724644.1:p.Val636Ala
XM_006724582.2:c.1907T>C	XP_006724645.1:p.Val636Ala
XM_006724583.2:c.1907T>C	XP_006724646.1:p.Val636Ala
XM_006724584.2:c.1907T>C	XP_006724647.1:p.Val636Ala
XM_011530772.1:c.1133T>C	XP_011529074.1:p.Val378Ala
XM_011530773.1:c.1100T>C	XP_011529075.1:p.Val367Ala
XM_011530774.1:c.1907T>C	XP_011529076.1:p.Val636Ala
XM_011530775.1:c.1907T>C	XP_011529077.1:p.Val636Ala
XM_011530776.1:c.1907T>C	XP_011529078.1:p.Val636Ala
XM_011530777.1:c.1907T>C	XP_011529079.1:p.Val636Ala
XR_938365.1:n.2134T>C
XM_006724579.3:c.1907T>C	XP_006724642.1:p.Val636Ala
XM_006724580.3:c.1196T>C	XP_006724643.1:p.Val399Ala
XM_006724581.4:c.1907T>C	XP_006724644.1:p.Val636Ala
XM_006724582.4:c.1907T>C	XP_006724645.1:p.Val636Ala
XM_006724583.4:c.1907T>C	XP_006724646.1:p.Val636Ala
XM_006724584.3:c.1907T>C	XP_006724647.1:p.Val636Ala
XM_011530773.2:c.1100T>C	XP_011529075.1:p.Val367Ala
XM_011530774.3:c.1907T>C	XP_011529076.1:p.Val636Ala
XM_011530776.2:c.1907T>C	XP_011529078.1:p.Val636Ala
XM_011530777.2:c.1907T>C	XP_011529079.1:p.Val636Ala
XM_017029359.2:c.1781T>C	XP_016884848.1:p.Val594Ala
XM_017029360.1:c.1313T>C	XP_016884849.1:p.Val438Ala
XR_938365.2:n.2128T>C
NM_001111125.3:c.1811T>C MANE Select	NP_001104595.1:p.Val604Ala
NM_015075.2:c.1196T>C	NP_055890.1:p.Val399Ala