Canonical Allele Identifier: CA812224274

Gene: CDC20B

Linked Data

• dbSNP Id: rs1447875554
• MyVariant Identifiers: chr5:g.54466473_54466475del (hg19) ; chr5:g.55170645_55170647del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55170650_55170652del , CM000667.2:g.55170650_55170652del	GRCh38
NC_000005.9:g.54466478_54466480del , CM000667.1:g.54466478_54466480del	GRCh37
NC_000005.8:g.54502235_54502237del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381375.7:c.126+1941_126+1943del MANE Select	ENSP00000370781.2:n.126+1941_126+1943del
ENST00000296733.5:c.126+1941_126+1943del	ENSP00000296733.1:n.126+1941_126+1943del
ENST00000322374.10:c.126+1941_126+1943del	ENSP00000315720.6:n.126+1941_126+1943del
ENST00000381375.6:c.126+1941_126+1943del	ENSP00000370781.2:n.126+1941_126+1943del
ENST00000507931.1:c.63+2291_63+2293del	ENSP00000423919.1:n.63+2291_63+2293del
ENST00000513180.5:c.126+1941_126+1943del	ENSP00000426776.1:n.126+1941_126+1943del
NM_001145734.2:c.126+1941_126+1943del	NP_001139206.2:n.126+1941_126+1943del
NM_001170402.1:c.126+1941_126+1943del MANE Select	NP_001163873.1:n.126+1941_126+1943del
NM_152623.2:c.126+1941_126+1943del	NP_689836.2:n.126+1941_126+1943del
XM_011543218.1:c.126+1941_126+1943del	XP_011541520.1:n.126+1941_126+1943del
XM_011543218.2:c.126+1941_126+1943del	XP_011541520.1:n.126+1941_126+1943del