Canonical Allele Identifier: CA82731923

Gene: IQCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121788719del , CM000665.2:g.121788719del	GRCh38
NC_000003.11:g.121507566del , CM000665.1:g.121507566del	GRCh37
NC_000003.10:g.122990256del	NCBI36
NG_015887.1:g.51377del

Transcript Alleles

HGVS	Amino-acid Change
NM_001023570.4:c.1130-271del MANE Select	NP_001018864.2:n.1130-271del
ENST00000310864.11:c.1130-271del MANE Select	ENSP00000311505.6:n.1130-271del
NM_001023570.2:c.1130-271del	NP_001018864.2:n.1130-271del
NM_001023570.3:c.1130-271del	NP_001018864.2:n.1130-271del
NM_001023571.2:c.731-271del	NP_001018865.2:n.731-271del
NM_001023571.3:c.731-271del	NP_001018865.2:n.731-271del
NM_001023571.4:c.731-271del	NP_001018865.2:n.731-271del
NM_001319107.1:c.1130-271del	NP_001306036.1:n.1130-271del
NM_001319107.2:c.1130-271del	NP_001306036.1:n.1130-271del
NR_134968.1:n.1234-271del
NR_134968.2:n.1215-271del
ENST00000310864.10:c.1130-271del	ENSP00000311505.6:n.1130-271del
ENST00000349820.10:c.731-271del	ENSP00000323756.7:n.731-271del
ENST00000393650.7:c.*108-271del	ENSP00000377261.3:n.*108-271del
XM_005247911.2:c.1130-271del	XP_005247968.1:n.1130-271del
XM_005247911.4:c.1130-271del	XP_005247968.1:n.1130-271del
XM_005247912.1:c.578-271del	XP_005247969.1:n.578-271del
XM_005247912.3:c.578-271del	XP_005247969.1:n.578-271del
XM_005247913.1:c.1129+1370del	XP_005247970.1:n.1129+1370del
XM_011513335.1:c.578-271del	XP_011511637.1:n.578-271del
XM_011513335.3:c.578-271del	XP_011511637.1:n.578-271del
XM_017007537.2:c.578-271del	XP_016863026.1:n.578-271del
XM_017007539.2:c.731-271del	XP_016863028.1:n.731-271del
XM_024453833.1:c.578-271del	XP_024309601.1:n.578-271del
XM_024453834.1:c.578-271del	XP_024309602.1:n.578-271del
XR_001740376.2:n.1257+1370del
XR_001740377.2:n.1257+1370del
XR_001740378.2:n.1148-271del
XR_001740379.2:n.1147+1370del
XR_001740380.2:n.1148-271del
XR_001740381.2:n.1147+1370del
XR_924221.1:n.1147-271del