Canonical Allele Identifier: CA1397658452

Gene: IQCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121781672_121781675delinsGTGT , CM000665.2:g.121781672_121781675delinsGTGT	GRCh38
NC_000003.11:g.121500519_121500522delinsGTGT , CM000665.1:g.121500519_121500522delinsGTGT	GRCh37
NC_000003.10:g.122983209_122983212delinsGTGT	NCBI36
NG_015887.1:g.58405_58408delinsACAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000310864.11:c.1410+68_1410+71delinsACAC MANE Select	ENSP00000311505.6:n.1410+68_1410+71delins...
ENST00000310864.10:c.1410+68_1410+71delinsACAC	ENSP00000311505.6:n.1410+68_1410+71delins...
ENST00000349820.10:c.1011+68_1011+71delinsACAC	ENSP00000323756.7:n.1011+68_1011+71delins...
ENST00000393650.7:c.*388+68_*388+71delinsACAC	ENSP00000377261.3:n.*388+68_*388+71delins...
NM_001023570.2:c.1410+68_1410+71delinsACAC	NP_001018864.2:n.1410+68_1410+71delinsACA...
NM_001023571.2:c.1011+68_1011+71delinsACAC	NP_001018865.2:n.1011+68_1011+71delinsACA...
XM_005247911.2:c.1410+68_1410+71delinsACAC	XP_005247968.1:n.1410+68_1410+71delinsACA...
XM_005247912.1:c.858+68_858+71delinsACAC	XP_005247969.1:n.858+68_858+71delinsACAC
XM_011513335.1:c.858+68_858+71delinsACAC	XP_011511637.1:n.858+68_858+71delinsACAC
XR_924221.1:n.1427+68_1427+71delinsACAC
NM_001023570.3:c.1410+68_1410+71delinsACAC	NP_001018864.2:n.1410+68_1410+71delinsACA...
NM_001023571.3:c.1011+68_1011+71delinsACAC	NP_001018865.2:n.1011+68_1011+71delinsACA...
NM_001319107.1:c.1410+68_1410+71delinsACAC	NP_001306036.1:n.1410+68_1410+71delinsACA...
NR_134968.1:n.1514+68_1514+71delinsACAC
XM_005247911.4:c.1410+68_1410+71delinsACAC	XP_005247968.1:n.1410+68_1410+71delinsACA...
XM_005247912.3:c.858+68_858+71delinsACAC	XP_005247969.1:n.858+68_858+71delinsACAC
XM_011513335.3:c.858+68_858+71delinsACAC	XP_011511637.1:n.858+68_858+71delinsACAC
XM_017007537.2:c.858+68_858+71delinsACAC	XP_016863026.1:n.858+68_858+71delinsACAC
XM_017007539.2:c.1011+68_1011+71delinsACAC	XP_016863028.1:n.1011+68_1011+71delinsACA...
XM_024453833.1:c.858+68_858+71delinsACAC	XP_024309601.1:n.858+68_858+71delinsACAC
XM_024453834.1:c.858+68_858+71delinsACAC	XP_024309602.1:n.858+68_858+71delinsACAC
XR_001740376.2:n.1389+68_1389+71delinsACAC
XR_001740377.2:n.1389+68_1389+71delinsACAC
XR_001740378.2:n.1428+68_1428+71delinsACAC
XR_001740379.2:n.1279+68_1279+71delinsACAC
XR_001740380.2:n.1428+68_1428+71delinsACAC
XR_001740381.2:n.1279+68_1279+71delinsACAC
NM_001023570.4:c.1410+68_1410+71delinsACAC MANE Select	NP_001018864.2:n.1410+68_1410+71delinsACA...
NM_001023571.4:c.1011+68_1011+71delinsACAC	NP_001018865.2:n.1011+68_1011+71delinsACA...
NM_001319107.2:c.1410+68_1410+71delinsACAC	NP_001306036.1:n.1410+68_1410+71delinsACA...
NR_134968.2:n.1495+68_1495+71delinsACAC