Canonical Allele Identifier: CA396308597

Gene: CTCF

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67611615T>G , CM000678.2:g.67611615T>G	GRCh38
NC_000016.9:g.67645518T>G , CM000678.1:g.67645518T>G	GRCh37
NC_000016.8:g.66203019T>G	NCBI36
NG_033892.1:g.54209T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264010.10:c.781+2T>G MANE Select	ENSP00000264010.4:n.781+2T>G
ENST00000401394.6:c.-32-5130T>G	ENSP00000384707.1:n.-32-5130T>G
ENST00000566078.2:n.787+2T>G
ENST00000642819.1:c.781+2T>G	ENSP00000494408.1:n.781+2T>G
ENST00000643892.1:c.781+2T>G	ENSP00000494358.1:n.781+2T>G
ENST00000644753.1:c.781+2T>G	ENSP00000493495.1:n.781+2T>G
ENST00000645306.1:c.781+2T>G	ENSP00000495218.1:n.781+2T>G
ENST00000645699.1:c.781+2T>G	ENSP00000495348.1:n.781+2T>G
ENST00000646076.1:c.781+2T>G	ENSP00000494538.1:n.781+2T>G
ENST00000646771.1:c.781+2T>G	ENSP00000494443.1:n.781+2T>G
ENST00000264010.8:c.781+2T>G	ENSP00000264010.4:n.781+2T>G
ENST00000401394.5:c.-32-5130T>G	ENSP00000384707.1:n.-32-5130T>G
ENST00000566078.1:n.1096T>G
NM_001191022.1:c.-32-5130T>G	NP_001177951.1:n.-32-5130T>G
NM_006565.3:c.781+2T>G	NP_006556.1:n.781+2T>G
XM_005255775.2:c.781+2T>G	XP_005255832.1:n.781+2T>G
NM_001363916.1:c.781+2T>G	NP_001350845.1:n.781+2T>G
XM_005255775.4:c.781+2T>G	XP_005255832.1:n.781+2T>G
XM_017022868.1:c.781+2T>G	XP_016878357.1:n.781+2T>G
NM_006565.4:c.781+2T>G MANE Select	NP_006556.1:n.781+2T>G
NM_001191022.2:c.-32-5130T>G	NP_001177951.1:n.-32-5130T>G