Canonical Allele Identifier: CA396311918

Gene: CTCF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67616771T>C , CM000678.2:g.67616771T>C	GRCh38
NC_000016.9:g.67650674T>C , CM000678.1:g.67650674T>C	GRCh37
NC_000016.8:g.66208175T>C	NCBI36
NG_033892.1:g.59365T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264010.10:c.979T>C MANE Select	ENSP00000264010.4:p.Cys327Arg
ENST00000401394.6:c.-6T>C	ENSP00000384707.1:n.-6T>C
ENST00000642819.1:c.979T>C	ENSP00000494408.1:p.Cys327Arg
ENST00000642943.1:n.2444T>C
ENST00000643892.1:c.979T>C	ENSP00000494358.1:p.Cys327Arg
ENST00000644753.1:c.979T>C	ENSP00000493495.1:p.Cys327Arg
ENST00000645306.1:c.979T>C	ENSP00000495218.1:p.Cys327Arg
ENST00000645409.1:n.1809T>C
ENST00000645699.1:c.979T>C	ENSP00000495348.1:p.Cys327Arg
ENST00000646076.1:c.979T>C	ENSP00000494538.1:p.Cys327Arg
ENST00000646566.1:n.1463T>C
ENST00000646771.1:c.979T>C	ENSP00000494443.1:p.Cys327Arg
ENST00000264010.8:c.979T>C	ENSP00000264010.4:p.Cys327Arg
ENST00000401394.5:c.-6T>C	ENSP00000384707.1:n.-6T>C
NM_001191022.1:c.-6T>C	NP_001177951.1:n.-6T>C
NM_006565.3:c.979T>C	NP_006556.1:p.Cys327Arg
XM_005255775.2:c.979T>C	XP_005255832.1:p.Cys327Arg
NM_001363916.1:c.979T>C	NP_001350845.1:p.Cys327Arg
XM_005255775.4:c.979T>C	XP_005255832.1:p.Cys327Arg
XM_017022868.1:c.979T>C	XP_016878357.1:p.Cys327Arg
NM_006565.4:c.979T>C MANE Select	NP_006556.1:p.Cys327Arg
NM_001191022.2:c.-6T>C	NP_001177951.1:n.-6T>C