Canonical Allele Identifier: CA8112764

Gene: CTCF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67629451G>A , CM000678.2:g.67629451G>A	GRCh38
NC_000016.9:g.67663354G>A , CM000678.1:g.67663354G>A	GRCh37
NC_000016.8:g.66220855G>A	NCBI36
NG_033892.1:g.72045G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006565.4:c.1755G>A MANE Select	NP_006556.1:p.Gly585=
ENST00000264010.10:c.1755G>A MANE Select	ENSP00000264010.4:p.Gly585=
NM_001191022.1:c.771G>A	NP_001177951.1:p.Gly257=
NM_001191022.2:c.771G>A	NP_001177951.1:p.Gly257=
NM_001363916.1:c.1755G>A	NP_001350845.1:p.Gly585=
NM_006565.3:c.1755G>A	NP_006556.1:p.Gly585=
ENST00000264010.8:c.1755G>A	ENSP00000264010.4:p.Gly585=
ENST00000401394.5:c.771G>A	ENSP00000384707.1:p.Gly257=
ENST00000401394.6:c.771G>A	ENSP00000384707.1:p.Gly257=
ENST00000642420.1:n.444G>A
ENST00000642819.1:c.1755G>A	ENSP00000494408.1:p.Gly585=
ENST00000643892.1:c.1755G>A	ENSP00000494358.1:p.Gly585=
ENST00000644753.1:c.1755G>A	ENSP00000493495.1:p.Gly585=
ENST00000644950.1:n.1103G>A
ENST00000645306.1:c.1755G>A	ENSP00000495218.1:p.Gly585=
ENST00000645409.1:n.2675G>A
ENST00000645699.1:c.1755G>A	ENSP00000495348.1:p.Gly585=
ENST00000646076.1:c.1755G>A	ENSP00000494538.1:p.Gly585=
ENST00000646566.1:n.2239G>A
ENST00000646771.1:c.1755G>A	ENSP00000494443.1:p.Gly585=
XM_005255775.2:c.1755G>A	XP_005255832.1:p.Gly585=
XM_005255775.4:c.1755G>A	XP_005255832.1:p.Gly585=
XM_017022868.1:c.1755G>A	XP_016878357.1:p.Gly585=