Canonical Allele Identifier: CA413149630

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53271064C>A (hg19) ; chrX:g.53241882C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241882C>A , CM000685.2:g.53241882C>A	GRCh38
NC_000023.10:g.53271064C>A , CM000685.1:g.53271064C>A	GRCh37
NC_000023.9:g.53287789C>A	NCBI36
NG_021296.1:g.84459G>T
NG_021296.2:g.84469G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3076G>T	ENSP00000516672.1:p.Val1026Phe
ENST00000638521.1:c.869G>T
ENST00000638869.1:c.378G>T
ENST00000639642.1:c.207G>T
ENST00000640694.1:c.2917G>T	ENSP00000492403.1:p.Val973Phe
ENST00000642864.1:c.2917G>T MANE Select	ENSP00000495726.1:p.Val973Phe
ENST00000674510.1:c.2917G>T	ENSP00000502054.1:p.Val973Phe
ENST00000674761.1:n.1224G>T
ENST00000675719.1:c.2887G>T	ENSP00000501927.1:p.Val963Phe
ENST00000375365.2:c.2302G>T	ENSP00000364514.2:p.Val768Phe
ENST00000396435.7:c.2917G>T	ENSP00000379712.3:p.Val973Phe
NM_001111125.2:c.2917G>T	NP_001104595.1:p.Val973Phe
NM_015075.1:c.2302G>T	NP_055890.1:p.Val768Phe
XM_006724579.2:c.3013G>T	XP_006724642.1:p.Val1005Phe
XM_006724580.2:c.2302G>T	XP_006724643.1:p.Val768Phe
XM_006724581.2:c.3013G>T	XP_006724644.1:p.Val1005Phe
XM_006724582.2:c.3013G>T	XP_006724645.1:p.Val1005Phe
XM_006724583.2:c.3013G>T	XP_006724646.1:p.Val1005Phe
XM_006724584.2:c.3013G>T	XP_006724647.1:p.Val1005Phe
XM_011530772.1:c.2239G>T	XP_011529074.1:p.Val747Phe
XM_011530773.1:c.2206G>T	XP_011529075.1:p.Val736Phe
XM_011530774.1:c.3013G>T	XP_011529076.1:p.Val1005Phe
XM_011530775.1:c.3013G>T	XP_011529077.1:p.Val1005Phe
XM_011530776.1:c.3013G>T	XP_011529078.1:p.Val1005Phe
XM_011530777.1:c.3013G>T	XP_011529079.1:p.Val1005Phe
XR_938365.1:n.3240G>T
XM_006724579.3:c.3013G>T	XP_006724642.1:p.Val1005Phe
XM_006724580.3:c.2302G>T	XP_006724643.1:p.Val768Phe
XM_006724581.4:c.3013G>T	XP_006724644.1:p.Val1005Phe
XM_006724582.4:c.3013G>T	XP_006724645.1:p.Val1005Phe
XM_006724583.4:c.3013G>T	XP_006724646.1:p.Val1005Phe
XM_006724584.3:c.3013G>T	XP_006724647.1:p.Val1005Phe
XM_011530773.2:c.2206G>T	XP_011529075.1:p.Val736Phe
XM_011530774.3:c.3013G>T	XP_011529076.1:p.Val1005Phe
XM_011530776.2:c.3013G>T	XP_011529078.1:p.Val1005Phe
XM_011530777.2:c.3013G>T	XP_011529079.1:p.Val1005Phe
XM_017029359.2:c.2887G>T	XP_016884848.1:p.Val963Phe
XM_017029360.1:c.2419G>T	XP_016884849.1:p.Val807Phe
XR_938365.2:n.3234G>T
NM_001111125.3:c.2917G>T MANE Select	NP_001104595.1:p.Val973Phe
NM_015075.2:c.2302G>T	NP_055890.1:p.Val768Phe