Canonical Allele Identifier: CA1397658498

Gene: IQCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121781772G= , CM000665.2:g.121781772G=	GRCh38
NC_000003.11:g.121500619G= , CM000665.1:g.121500619G=	GRCh37
NC_000003.10:g.122983309G=	NCBI36
NG_015887.1:g.58308C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310864.11:c.1381C= MANE Select	ENSP00000311505.6:p.Arg461=
ENST00000310864.10:c.1381C=	ENSP00000311505.6:p.Arg461=
ENST00000349820.10:c.982C=	ENSP00000323756.7:p.Arg328=
ENST00000393650.7:c.*359C=	ENSP00000377261.3:n.*359C=
NM_001023570.2:c.1381C=	NP_001018864.2:p.Arg461=
NM_001023571.2:c.982C=	NP_001018865.2:p.Arg328=
XM_005247911.2:c.1381C=	XP_005247968.1:p.Arg461=
XM_005247912.1:c.829C=	XP_005247969.1:p.Arg277=
XM_005247913.1:c.*95C=	XP_005247970.1:n.*95C=
XM_011513335.1:c.829C=	XP_011511637.1:p.Arg277=
XR_924221.1:n.1398C=
NM_001023570.3:c.1381C=	NP_001018864.2:p.Arg461=
NM_001023571.3:c.982C=	NP_001018865.2:p.Arg328=
NM_001319107.1:c.1381C=	NP_001306036.1:p.Arg461=
NR_134968.1:n.1485C=
XM_005247911.4:c.1381C=	XP_005247968.1:p.Arg461=
XM_005247912.3:c.829C=	XP_005247969.1:p.Arg277=
XM_011513335.3:c.829C=	XP_011511637.1:p.Arg277=
XM_017007537.2:c.829C=	XP_016863026.1:p.Arg277=
XM_017007539.2:c.982C=	XP_016863028.1:p.Arg328=
XM_024453833.1:c.829C=	XP_024309601.1:p.Arg277=
XM_024453834.1:c.829C=	XP_024309602.1:p.Arg277=
XR_001740376.2:n.1360C=
XR_001740377.2:n.1360C=
XR_001740378.2:n.1399C=
XR_001740379.2:n.1250C=
XR_001740380.2:n.1399C=
XR_001740381.2:n.1250C=
NM_001023570.4:c.1381C= MANE Select	NP_001018864.2:p.Arg461=
NM_001023571.4:c.982C=	NP_001018865.2:p.Arg328=
NM_001319107.2:c.1381C=	NP_001306036.1:p.Arg461=
NR_134968.2:n.1466C=