Canonical Allele Identifier: CA10603332
Gene: CTCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67611442dup , CM000678.2:g.67611442dup GRCh38
NC_000016.9:g.67645345dup , CM000678.1:g.67645345dup GRCh37
NC_000016.8:g.66202846dup NCBI36
NG_033892.1:g.54036dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264010.10:c.610dup MANE Select ENSP00000264010.4:p.Thr204AsnfsTer26
ENST00000401394.6:c.-32-5303dup ENSP00000384707.1:n.-32-5303dup
ENST00000566078.2:n.616dup
ENST00000642819.1:c.610dup ENSP00000494408.1:p.Thr204AsnfsTer26
ENST00000643892.1:c.610dup ENSP00000494358.1:p.Thr204AsnfsTer26
ENST00000644753.1:c.610dup ENSP00000493495.1:p.Thr204AsnfsTer26
ENST00000645306.1:c.610dup ENSP00000495218.1:p.Thr204AsnfsTer26
ENST00000645699.1:c.610dup ENSP00000495348.1:p.Thr204AsnfsTer26
ENST00000646076.1:c.610dup ENSP00000494538.1:p.Thr204AsnfsTer26
ENST00000646771.1:c.610dup ENSP00000494443.1:p.Thr204AsnfsTer26
ENST00000264010.8:c.610dup ENSP00000264010.4:p.Thr204AsnfsTer26
ENST00000401394.5:c.-32-5303dup ENSP00000384707.1:n.-32-5303dup
ENST00000566078.1:n.923dup
NM_001191022.1:c.-32-5303dup NP_001177951.1:n.-32-5303dup
NM_006565.3:c.610dup NP_006556.1:p.Thr204AsnfsTer26
XM_005255775.2:c.610dup XP_005255832.1:p.Thr204AsnfsTer26
NM_001363916.1:c.610dup NP_001350845.1:p.Thr204AsnfsTer26
XM_005255775.4:c.610dup XP_005255832.1:p.Thr204AsnfsTer26
XM_017022868.1:c.610dup XP_016878357.1:p.Thr204AsnfsTer26
NM_006565.4:c.610dup MANE Select NP_006556.1:p.Thr204AsnfsTer26
NM_001191022.2:c.-32-5303dup NP_001177951.1:n.-32-5303dup
Search 100 bp 5'
Search 100 bp 3'