Canonical Allele Identifier: CA2429775094

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248864G= , CM000685.2:g.53248864G=	GRCh38
NC_000023.10:g.53278046G= , CM000685.1:g.53278046G=	GRCh37
NC_000023.9:g.53294771G=	NCBI36
NG_021296.1:g.77477C=
NG_021296.2:g.77487C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2475C=	ENSP00000516672.1:p.Ile825=
ENST00000638521.1:c.268C=
ENST00000640694.1:c.2316C=	ENSP00000492403.1:p.Ile772=
ENST00000642864.1:c.2316C= MANE Select	ENSP00000495726.1:p.Ile772=
ENST00000674510.1:c.2316C=	ENSP00000502054.1:p.Ile772=
ENST00000675719.1:c.2286C=	ENSP00000501927.1:p.Ile762=
ENST00000375365.2:c.1701C=	ENSP00000364514.2:p.Ile567=
ENST00000396435.7:c.2316C=	ENSP00000379712.3:p.Ile772=
NM_001111125.2:c.2316C=	NP_001104595.1:p.Ile772=
NM_015075.1:c.1701C=	NP_055890.1:p.Ile567=
XM_006724579.2:c.2412C=	XP_006724642.1:p.Ile804=
XM_006724580.2:c.1701C=	XP_006724643.1:p.Ile567=
XM_006724581.2:c.2412C=	XP_006724644.1:p.Ile804=
XM_006724582.2:c.2412C=	XP_006724645.1:p.Ile804=
XM_006724583.2:c.2412C=	XP_006724646.1:p.Ile804=
XM_006724584.2:c.2412C=	XP_006724647.1:p.Ile804=
XM_011530772.1:c.1638C=	XP_011529074.1:p.Ile546=
XM_011530773.1:c.1605C=	XP_011529075.1:p.Ile535=
XM_011530774.1:c.2412C=	XP_011529076.1:p.Ile804=
XM_011530775.1:c.2412C=	XP_011529077.1:p.Ile804=
XM_011530776.1:c.2412C=	XP_011529078.1:p.Ile804=
XM_011530777.1:c.2412C=	XP_011529079.1:p.Ile804=
XR_938365.1:n.2639C=
XM_006724579.3:c.2412C=	XP_006724642.1:p.Ile804=
XM_006724580.3:c.1701C=	XP_006724643.1:p.Ile567=
XM_006724581.4:c.2412C=	XP_006724644.1:p.Ile804=
XM_006724582.4:c.2412C=	XP_006724645.1:p.Ile804=
XM_006724583.4:c.2412C=	XP_006724646.1:p.Ile804=
XM_006724584.3:c.2412C=	XP_006724647.1:p.Ile804=
XM_011530773.2:c.1605C=	XP_011529075.1:p.Ile535=
XM_011530774.3:c.2412C=	XP_011529076.1:p.Ile804=
XM_011530776.2:c.2412C=	XP_011529078.1:p.Ile804=
XM_011530777.2:c.2412C=	XP_011529079.1:p.Ile804=
XM_017029359.2:c.2286C=	XP_016884848.1:p.Ile762=
XM_017029360.1:c.1818C=	XP_016884849.1:p.Ile606=
XR_938365.2:n.2633C=
NM_001111125.3:c.2316C= MANE Select	NP_001104595.1:p.Ile772=
NM_015075.2:c.1701C=	NP_055890.1:p.Ile567=