Canonical Allele Identifier: CA1547364603
Gene: CDC20B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55170644_55170647delinsCAAG , CM000667.2:g.55170644_55170647delinsCAAG GRCh38
NC_000005.9:g.54466472_54466475delinsCAAG , CM000667.1:g.54466472_54466475delinsCAAG GRCh37
NC_000005.8:g.54502229_54502232delinsCAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381375.7:c.126+1941_126+1944delinsCTTG MANE Select ENSP00000370781.2:n.126+1941_126+1944delinsCTTG
ENST00000296733.5:c.126+1941_126+1944delinsCTTG ENSP00000296733.1:n.126+1941_126+1944delinsCTTG
ENST00000322374.10:c.126+1941_126+1944delinsCTTG ENSP00000315720.6:n.126+1941_126+1944delinsCTTG
ENST00000381375.6:c.126+1941_126+1944delinsCTTG ENSP00000370781.2:n.126+1941_126+1944delinsCTTG
ENST00000507931.1:c.63+2291_63+2294delinsCTTG ENSP00000423919.1:n.63+2291_63+2294delinsCTTG
ENST00000513180.5:c.126+1941_126+1944delinsCTTG ENSP00000426776.1:n.126+1941_126+1944delinsCTTG
NM_001145734.2:c.126+1941_126+1944delinsCTTG NP_001139206.2:n.126+1941_126+1944delinsCTTG
NM_001170402.1:c.126+1941_126+1944delinsCTTG MANE Select NP_001163873.1:n.126+1941_126+1944delinsCTTG
NM_152623.2:c.126+1941_126+1944delinsCTTG NP_689836.2:n.126+1941_126+1944delinsCTTG
XM_011543218.1:c.126+1941_126+1944delinsCTTG XP_011541520.1:n.126+1941_126+1944delinsCTTG
XM_011543218.2:c.126+1941_126+1944delinsCTTG XP_011541520.1:n.126+1941_126+1944delinsCTTG