Canonical Allele Identifier: CA10614589

Gene: IQCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121770148C>G , CM000665.2:g.121770148C>G	GRCh38
NC_000003.11:g.121488995C>G , CM000665.1:g.121488995C>G	GRCh37
NC_000003.10:g.122971685C>G	NCBI36
NG_015887.1:g.69932G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001023570.4:c.*197G>C MANE Select	NP_001018864.2:n.*197G>C
ENST00000310864.11:c.*197G>C MANE Select	ENSP00000311505.6:n.*197G>C
NM_001023570.2:c.*197G>C	NP_001018864.2:n.*197G>C
NM_001023570.3:c.*197G>C	NP_001018864.2:n.*197G>C
NM_001023571.2:c.*197G>C	NP_001018865.2:n.*197G>C
NM_001023571.3:c.*197G>C	NP_001018865.2:n.*197G>C
NM_001023571.4:c.*197G>C	NP_001018865.2:n.*197G>C
NM_001319107.1:c.*197G>C	NP_001306036.1:n.*197G>C
NM_001319107.2:c.*197G>C	NP_001306036.1:n.*197G>C
NR_134968.1:n.2098G>C
NR_134968.2:n.2079G>C
ENST00000310864.10:c.*197G>C	ENSP00000311505.6:n.*197G>C
ENST00000349820.10:c.*197G>C	ENSP00000323756.7:n.*197G>C
ENST00000393650.7:c.*972G>C	ENSP00000377261.3:n.*972G>C
XM_005247911.2:c.*412G>C	XP_005247968.1:n.*412G>C
XM_005247911.4:c.*412G>C	XP_005247968.1:n.*412G>C
XM_005247912.1:c.*197G>C	XP_005247969.1:n.*197G>C
XM_005247912.3:c.*197G>C	XP_005247969.1:n.*197G>C
XM_011513335.1:c.*197G>C	XP_011511637.1:n.*197G>C
XM_011513335.3:c.*197G>C	XP_011511637.1:n.*197G>C
XM_017007537.2:c.*197G>C	XP_016863026.1:n.*197G>C
XM_017007539.2:c.*412G>C	XP_016863028.1:n.*412G>C
XM_024453833.1:c.*197G>C	XP_024309601.1:n.*197G>C
XM_024453834.1:c.*197G>C	XP_024309602.1:n.*197G>C
XR_001740376.2:n.1973G>C
XR_001740377.2:n.1816G>C
XR_001740378.2:n.2012G>C
XR_001740379.2:n.1863G>C
XR_001740380.2:n.1855G>C
XR_001740381.2:n.1706G>C
XR_924221.1:n.2011G>C