Canonical Allele Identifier: CA2429775644

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250803A= , CM000685.2:g.53250803A=	GRCh38
NC_000023.10:g.53279985A= , CM000685.1:g.53279985A=	GRCh37
NC_000023.9:g.53296710A=	NCBI36
NG_021296.1:g.75538T=
NG_021296.2:g.75548T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1932T=	ENSP00000516672.1:p.Leu644=
ENST00000640694.1:c.1773T=	ENSP00000492403.1:p.Leu591=
ENST00000642864.1:c.1773T= MANE Select	ENSP00000495726.1:p.Leu591=
ENST00000674510.1:c.1773T=	ENSP00000502054.1:p.Leu591=
ENST00000675719.1:c.1743T=	ENSP00000501927.1:p.Leu581=
ENST00000375365.2:c.1158T=	ENSP00000364514.2:p.Leu386=
ENST00000396435.7:c.1773T=	ENSP00000379712.3:p.Leu591=
NM_001111125.2:c.1773T=	NP_001104595.1:p.Leu591=
NM_015075.1:c.1158T=	NP_055890.1:p.Leu386=
XM_006724579.2:c.1869T=	XP_006724642.1:p.Leu623=
XM_006724580.2:c.1158T=	XP_006724643.1:p.Leu386=
XM_006724581.2:c.1869T=	XP_006724644.1:p.Leu623=
XM_006724582.2:c.1869T=	XP_006724645.1:p.Leu623=
XM_006724583.2:c.1869T=	XP_006724646.1:p.Leu623=
XM_006724584.2:c.1869T=	XP_006724647.1:p.Leu623=
XM_011530772.1:c.1095T=	XP_011529074.1:p.Leu365=
XM_011530773.1:c.1062T=	XP_011529075.1:p.Leu354=
XM_011530774.1:c.1869T=	XP_011529076.1:p.Leu623=
XM_011530775.1:c.1869T=	XP_011529077.1:p.Leu623=
XM_011530776.1:c.1869T=	XP_011529078.1:p.Leu623=
XM_011530777.1:c.1869T=	XP_011529079.1:p.Leu623=
XR_938365.1:n.2096T=
XM_006724579.3:c.1869T=	XP_006724642.1:p.Leu623=
XM_006724580.3:c.1158T=	XP_006724643.1:p.Leu386=
XM_006724581.4:c.1869T=	XP_006724644.1:p.Leu623=
XM_006724582.4:c.1869T=	XP_006724645.1:p.Leu623=
XM_006724583.4:c.1869T=	XP_006724646.1:p.Leu623=
XM_006724584.3:c.1869T=	XP_006724647.1:p.Leu623=
XM_011530773.2:c.1062T=	XP_011529075.1:p.Leu354=
XM_011530774.3:c.1869T=	XP_011529076.1:p.Leu623=
XM_011530776.2:c.1869T=	XP_011529078.1:p.Leu623=
XM_011530777.2:c.1869T=	XP_011529079.1:p.Leu623=
XM_017029359.2:c.1743T=	XP_016884848.1:p.Leu581=
XM_017029360.1:c.1275T=	XP_016884849.1:p.Leu425=
XR_938365.2:n.2090T=
NM_001111125.3:c.1773T= MANE Select	NP_001104595.1:p.Leu591=
NM_015075.2:c.1158T=	NP_055890.1:p.Leu386=