Canonical Allele Identifier: CA8112603
Gene: CTCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67616761G>A , CM000678.2:g.67616761G>A GRCh38
NC_000016.9:g.67650664G>A , CM000678.1:g.67650664G>A GRCh37
NC_000016.8:g.66208165G>A NCBI36
NG_033892.1:g.59355G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264010.10:c.969G>A MANE Select ENSP00000264010.4:p.Lys323=
ENST00000401394.6:c.-16G>A ENSP00000384707.1:n.-16G>A
ENST00000642819.1:c.969G>A ENSP00000494408.1:p.Lys323=
ENST00000642943.1:n.2434G>A
ENST00000643892.1:c.969G>A ENSP00000494358.1:p.Lys323=
ENST00000644753.1:c.969G>A ENSP00000493495.1:p.Lys323=
ENST00000645306.1:c.969G>A ENSP00000495218.1:p.Lys323=
ENST00000645409.1:n.1799G>A
ENST00000645699.1:c.969G>A ENSP00000495348.1:p.Lys323=
ENST00000646076.1:c.969G>A ENSP00000494538.1:p.Lys323=
ENST00000646566.1:n.1453G>A
ENST00000646771.1:c.969G>A ENSP00000494443.1:p.Lys323=
ENST00000264010.8:c.969G>A ENSP00000264010.4:p.Lys323=
ENST00000401394.5:c.-16G>A ENSP00000384707.1:n.-16G>A
NM_001191022.1:c.-16G>A NP_001177951.1:n.-16G>A
NM_006565.3:c.969G>A NP_006556.1:p.Lys323=
XM_005255775.2:c.969G>A XP_005255832.1:p.Lys323=
NM_001363916.1:c.969G>A NP_001350845.1:p.Lys323=
XM_005255775.4:c.969G>A XP_005255832.1:p.Lys323=
XM_017022868.1:c.969G>A XP_016878357.1:p.Lys323=
NM_006565.4:c.969G>A MANE Select NP_006556.1:p.Lys323=
NM_001191022.2:c.-16G>A NP_001177951.1:n.-16G>A