Canonical Allele Identifier: CA413141954

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53264243A>G (hg19) ; chrX:g.53235061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235061A>G , CM000685.2:g.53235061A>G	GRCh38
NC_000023.10:g.53264243A>G , CM000685.1:g.53264243A>G	GRCh37
NC_000023.9:g.53280968A>G	NCBI36
NG_021296.1:g.91280T>C
NG_021296.2:g.91290T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3784T>C	ENSP00000516672.1:p.Phe1262Leu
ENST00000638521.1:c.1453+722T>C
ENST00000638869.1:c.962+722T>C
ENST00000639796.1:c.316+1261T>C	ENSP00000492252.1:n.316+1261T>C
ENST00000640005.1:c.514+1261T>C	ENSP00000491293.1:n.514+1261T>C
ENST00000640694.1:c.*110T>C	ENSP00000492403.1:n.*110T>C
ENST00000642864.1:c.3625T>C MANE Select	ENSP00000495726.1:p.Phe1209Leu
ENST00000674510.1:c.3625T>C	ENSP00000502054.1:p.Phe1209Leu
ENST00000675719.1:c.3595T>C	ENSP00000501927.1:p.Phe1199Leu
ENST00000375365.2:c.*110T>C	ENSP00000364514.2:n.*110T>C
ENST00000396435.7:c.3625T>C	ENSP00000379712.3:p.Phe1209Leu
NM_001111125.2:c.3625T>C	NP_001104595.1:p.Phe1209Leu
NM_015075.1:c.*110T>C	NP_055890.1:n.*110T>C
XM_006724579.2:c.3721T>C	XP_006724642.1:p.Phe1241Leu
XM_006724580.2:c.3010T>C	XP_006724643.1:p.Phe1004Leu
XM_006724581.2:c.3597+722T>C	XP_006724644.1:n.3597+722T>C
XM_006724582.2:c.3597+722T>C	XP_006724645.1:n.3597+722T>C
XM_006724583.2:c.3547+1261T>C	XP_006724646.1:n.3547+1261T>C
XM_006724584.2:c.*110T>C	XP_006724647.1:n.*110T>C
XM_011530772.1:c.2947T>C	XP_011529074.1:p.Phe983Leu
XM_011530773.1:c.2914T>C	XP_011529075.1:p.Phe972Leu
XM_011530775.1:c.3547+1261T>C	XP_011529077.1:n.3547+1261T>C
XM_006724579.3:c.3721T>C	XP_006724642.1:p.Phe1241Leu
XM_006724580.3:c.3010T>C	XP_006724643.1:p.Phe1004Leu
XM_006724581.4:c.3597+722T>C	XP_006724644.1:n.3597+722T>C
XM_006724582.4:c.3597+722T>C	XP_006724645.1:n.3597+722T>C
XM_006724583.4:c.3547+1261T>C	XP_006724646.1:n.3547+1261T>C
XM_006724584.3:c.*110T>C	XP_006724647.1:n.*110T>C
XM_011530773.2:c.2914T>C	XP_011529075.1:p.Phe972Leu
XM_017029359.2:c.3595T>C	XP_016884848.1:p.Phe1199Leu
XM_017029360.1:c.3127T>C	XP_016884849.1:p.Phe1043Leu
NM_001111125.3:c.3625T>C MANE Select	NP_001104595.1:p.Phe1209Leu
NM_015075.2:c.*110T>C	NP_055890.1:n.*110T>C