Canonical Allele Identifier: CA396324431

Gene: CTCF

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67636852G>T , CM000678.2:g.67636852G>T	GRCh38
NC_000016.9:g.67670755G>T , CM000678.1:g.67670755G>T	GRCh37
NC_000016.8:g.66228256G>T	NCBI36
NG_033892.1:g.79446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264010.10:c.1999+1G>T MANE Select	ENSP00000264010.4:n.1999+1G>T
ENST00000401394.6:c.1015+1G>T	ENSP00000384707.1:n.1015+1G>T
ENST00000642420.1:n.688+1G>T
ENST00000642819.1:c.1999+1G>T	ENSP00000494408.1:n.1999+1G>T
ENST00000643892.1:c.*200+1G>T	ENSP00000494358.1:n.*200+1G>T
ENST00000644753.1:c.1999+1G>T	ENSP00000493495.1:n.1999+1G>T
ENST00000644950.1:n.1347+1G>T
ENST00000645306.1:c.1999+1G>T	ENSP00000495218.1:n.1999+1G>T
ENST00000645409.1:n.2919+1G>T
ENST00000645699.1:c.1999+1G>T	ENSP00000495348.1:n.1999+1G>T
ENST00000646076.1:c.1999+1G>T	ENSP00000494538.1:n.1999+1G>T
ENST00000646566.1:n.2483+1G>T
ENST00000646771.1:c.1999+1G>T	ENSP00000494443.1:n.1999+1G>T
ENST00000264010.8:c.1999+1G>T	ENSP00000264010.4:n.1999+1G>T
ENST00000401394.5:c.1015+1G>T	ENSP00000384707.1:n.1015+1G>T
NM_001191022.1:c.1015+1G>T	NP_001177951.1:n.1015+1G>T
NM_006565.3:c.1999+1G>T	NP_006556.1:n.1999+1G>T
XM_005255775.2:c.1999+1G>T	XP_005255832.1:n.1999+1G>T
NM_001363916.1:c.1999+1G>T	NP_001350845.1:n.1999+1G>T
XM_005255775.4:c.1999+1G>T	XP_005255832.1:n.1999+1G>T
XM_017022868.1:c.1999+1G>T	XP_016878357.1:n.1999+1G>T
NM_006565.4:c.1999+1G>T MANE Select	NP_006556.1:n.1999+1G>T
NM_001191022.2:c.1015+1G>T	NP_001177951.1:n.1015+1G>T