Canonical Allele Identifier: CA1914240063
Gene: CABCOCO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61764775G= , CM000672.2:g.61764775G= GRCh38
NC_000010.10:g.63524533G= , CM000672.1:g.63524533G= GRCh37
NC_000010.9:g.63194539G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000648843.3:c.817-1164G= MANE Select ENSP00000496918.2:n.817-1164G=
ENST00000330194.2:c.553-1164G= ENSP00000328698.2:n.553-1164G=
NM_173554.2:c.553-1164G= NP_775825.1:n.553-1164G=
XM_005269598.2:c.679-1164G= XP_005269655.1:n.679-1164G=
XM_005269599.3:c.679-1164G= XP_005269656.1:n.679-1164G=
XM_005269600.3:c.553-1164G= XP_005269657.1:n.553-1164G=
XM_006717690.2:c.817-1164G= XP_006717753.1:n.817-1164G=
NM_001366905.1:c.553-1164G= NP_001353834.1:n.553-1164G=
NM_001366906.1:c.817-1164G= NP_001353835.1:n.817-1164G=
NM_001366908.1:c.679-1164G= NP_001353837.1:n.679-1164G=
XM_005269598.3:c.679-1164G= XP_005269655.1:n.679-1164G=
NM_001366905.2:c.553-1164G= NP_001353834.1:n.553-1164G=
NM_001366906.2:c.817-1164G= MANE Select NP_001353835.1:n.817-1164G=
NM_001366908.2:c.679-1164G= NP_001353837.1:n.679-1164G=
NM_173554.3:c.553-1164G= NP_775825.1:n.553-1164G=