Canonical Allele Identifier: CA2229415544

Gene: CTCF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67628550C= , CM000678.2:g.67628550C=	GRCh38
NC_000016.9:g.67662453C= , CM000678.1:g.67662453C=	GRCh37
NC_000016.8:g.66219954C=	NCBI36
NG_033892.1:g.71144C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264010.10:c.1699C= MANE Select	ENSP00000264010.4:p.Arg567=
ENST00000401394.6:c.715C=	ENSP00000384707.1:p.Arg239=
ENST00000642420.1:n.388C=
ENST00000642819.1:c.1699C=	ENSP00000494408.1:p.Arg567=
ENST00000643892.1:c.1699C=	ENSP00000494358.1:p.Arg567=
ENST00000644753.1:c.1699C=	ENSP00000493495.1:p.Arg567=
ENST00000644950.1:n.1047C=
ENST00000645306.1:c.1699C=	ENSP00000495218.1:p.Arg567=
ENST00000645409.1:n.2619C=
ENST00000645699.1:c.1699C=	ENSP00000495348.1:p.Arg567=
ENST00000646076.1:c.1699C=	ENSP00000494538.1:p.Arg567=
ENST00000646566.1:n.2183C=
ENST00000646771.1:c.1699C=	ENSP00000494443.1:p.Arg567=
ENST00000264010.8:c.1699C=	ENSP00000264010.4:p.Arg567=
ENST00000401394.5:c.715C=	ENSP00000384707.1:p.Arg239=
NM_001191022.1:c.715C=	NP_001177951.1:p.Arg239=
NM_006565.3:c.1699C=	NP_006556.1:p.Arg567=
XM_005255775.2:c.1699C=	XP_005255832.1:p.Arg567=
NM_001363916.1:c.1699C=	NP_001350845.1:p.Arg567=
XM_005255775.4:c.1699C=	XP_005255832.1:p.Arg567=
XM_017022868.1:c.1699C=	XP_016878357.1:p.Arg567=
NM_006565.4:c.1699C= MANE Select	NP_006556.1:p.Arg567=
NM_001191022.2:c.715C=	NP_001177951.1:p.Arg239=