Canonical Allele Identifier: CA2567077

Gene: IQCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121772615G>C , CM000665.2:g.121772615G>C	GRCh38
NC_000003.11:g.121491462G>C , CM000665.1:g.121491462G>C	GRCh37
NC_000003.10:g.122974152G>C	NCBI36
NG_015887.1:g.67465C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001023570.4:c.1509C>G MANE Select	NP_001018864.2:p.Ala503=
ENST00000310864.11:c.1509C>G MANE Select	ENSP00000311505.6:p.Ala503=
NM_001023570.2:c.1509C>G	NP_001018864.2:p.Ala503=
NM_001023570.3:c.1509C>G	NP_001018864.2:p.Ala503=
NM_001023571.2:c.1110C>G	NP_001018865.2:p.Ala370=
NM_001023571.3:c.1110C>G	NP_001018865.2:p.Ala370=
NM_001023571.4:c.1110C>G	NP_001018865.2:p.Ala370=
NM_001319107.1:c.1509C>G	NP_001306036.1:p.Ala503=
NM_001319107.2:c.1509C>G	NP_001306036.1:p.Ala503=
NR_134968.1:n.1613C>G
NR_134968.2:n.1594C>G
ENST00000310864.10:c.1509C>G	ENSP00000311505.6:p.Ala503=
ENST00000349820.10:c.1110C>G	ENSP00000323756.7:p.Ala370=
ENST00000393650.7:c.*487C>G	ENSP00000377261.3:n.*487C>G
XM_005247911.2:c.1411-2041C>G	XP_005247968.1:n.1411-2041C>G
XM_005247911.4:c.1411-2041C>G	XP_005247968.1:n.1411-2041C>G
XM_005247912.1:c.957C>G	XP_005247969.1:p.Ala319=
XM_005247912.3:c.957C>G	XP_005247969.1:p.Ala319=
XM_011513335.1:c.957C>G	XP_011511637.1:p.Ala319=
XM_011513335.3:c.957C>G	XP_011511637.1:p.Ala319=
XM_017007537.2:c.957C>G	XP_016863026.1:p.Ala319=
XM_017007539.2:c.1012-2041C>G	XP_016863028.1:n.1012-2041C>G
XM_024453833.1:c.957C>G	XP_024309601.1:p.Ala319=
XM_024453834.1:c.957C>G	XP_024309602.1:p.Ala319=
XR_001740376.2:n.1488C>G
XR_001740377.2:n.1390-2041C>G
XR_001740378.2:n.1527C>G
XR_001740379.2:n.1378C>G
XR_001740380.2:n.1429-2041C>G
XR_001740381.2:n.1280-2041C>G
XR_924221.1:n.1526C>G