Canonical Allele Identifier: CA2429777177

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53255845G= , CM000685.2:g.53255845G=	GRCh38
NC_000023.10:g.53285027G= , CM000685.1:g.53285027G=	GRCh37
NC_000023.9:g.53301752G=	NCBI36
NG_021296.1:g.70496C=
NG_021296.2:g.70506C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1113C=	ENSP00000516672.1:p.Ala371=
ENST00000638630.1:c.243C=	ENSP00000492390.1:p.Ala81=
ENST00000640694.1:c.954C=	ENSP00000492403.1:p.Ala318=
ENST00000642864.1:c.954C= MANE Select	ENSP00000495726.1:p.Ala318=
ENST00000674510.1:c.954C=	ENSP00000502054.1:p.Ala318=
ENST00000675719.1:c.924C=	ENSP00000501927.1:p.Ala308=
ENST00000375365.2:c.339C=	ENSP00000364514.2:p.Ala113=
ENST00000396435.7:c.954C=	ENSP00000379712.3:p.Ala318=
NM_001111125.2:c.954C=	NP_001104595.1:p.Ala318=
NM_015075.1:c.339C=	NP_055890.1:p.Ala113=
XM_006724579.2:c.1050C=	XP_006724642.1:p.Ala350=
XM_006724580.2:c.339C=	XP_006724643.1:p.Ala113=
XM_006724581.2:c.1050C=	XP_006724644.1:p.Ala350=
XM_006724582.2:c.1050C=	XP_006724645.1:p.Ala350=
XM_006724583.2:c.1050C=	XP_006724646.1:p.Ala350=
XM_006724584.2:c.1050C=	XP_006724647.1:p.Ala350=
XM_011530772.1:c.276C=	XP_011529074.1:p.Ala92=
XM_011530773.1:c.243C=	XP_011529075.1:p.Ala81=
XM_011530774.1:c.1050C=	XP_011529076.1:p.Ala350=
XM_011530775.1:c.1050C=	XP_011529077.1:p.Ala350=
XM_011530776.1:c.1050C=	XP_011529078.1:p.Ala350=
XM_011530777.1:c.1050C=	XP_011529079.1:p.Ala350=
XR_938365.1:n.1277C=
XM_006724579.3:c.1050C=	XP_006724642.1:p.Ala350=
XM_006724580.3:c.339C=	XP_006724643.1:p.Ala113=
XM_006724581.4:c.1050C=	XP_006724644.1:p.Ala350=
XM_006724582.4:c.1050C=	XP_006724645.1:p.Ala350=
XM_006724583.4:c.1050C=	XP_006724646.1:p.Ala350=
XM_006724584.3:c.1050C=	XP_006724647.1:p.Ala350=
XM_011530773.2:c.243C=	XP_011529075.1:p.Ala81=
XM_011530774.3:c.1050C=	XP_011529076.1:p.Ala350=
XM_011530776.2:c.1050C=	XP_011529078.1:p.Ala350=
XM_011530777.2:c.1050C=	XP_011529079.1:p.Ala350=
XM_017029359.2:c.924C=	XP_016884848.1:p.Ala308=
XM_017029360.1:c.456C=	XP_016884849.1:p.Ala152=
XR_938365.2:n.1271C=
NM_001111125.3:c.954C= MANE Select	NP_001104595.1:p.Ala318=
NM_015075.2:c.339C=	NP_055890.1:p.Ala113=