Canonical Allele Identifier: CA1308216369

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366223_173366224delinsAT , CM000664.2:g.173366223_173366224delinsAT	GRCh38
NC_000002.11:g.174230951_174230952delinsAT , CM000664.1:g.174230951_174230952delinsAT	GRCh37
NC_000002.10:g.173939197_173939198delinsAT	NCBI36
NG_047202.1:g.17207_17208delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+631_798+632delinsAT	ENSP00000512251.1:n.798+631_798+632delinsAT
ENST00000695911.1:c.814-60_814-59delinsAT	ENSP00000512262.1:n.814-60_814-59delinsAT
ENST00000695912.1:c.1033-60_1033-59delinsAT	ENSP00000512263.1:n.1033-60_1033-59delinsAT
ENST00000695913.1:c.*1729_*1730delinsAT	ENSP00000512264.1:n.*1729_*1730delinsAT
ENST00000695914.1:c.796-60_796-59delinsAT	ENSP00000512265.1:n.796-60_796-59delinsAT
ENST00000695918.1:n.264-60_264-59delinsAT
ENST00000306721.8:c.1036-60_1036-59delinsAT MANE Select	ENSP00000306968.3:n.1036-60_1036-59delinsAT
ENST00000306721.7:c.1036-60_1036-59delinsAT	ENSP00000306968.3:n.1036-60_1036-59delinsAT
ENST00000347703.7:c.799-60_799-59delinsAT	ENSP00000272789.4:n.799-60_799-59delinsAT
ENST00000410019.3:c.673-60_673-59delinsAT	ENSP00000386833.3:n.673-60_673-59delinsAT
ENST00000410101.7:c.904-60_904-59delinsAT	ENSP00000386656.3:n.904-60_904-59delinsAT
ENST00000467411.5:n.1768+631_1768+632delinsAT
ENST00000496441.5:n.1790-60_1790-59delinsAT
NM_031942.4:c.1036-60_1036-59delinsAT	NP_114148.3:n.1036-60_1036-59delinsAT
NM_145810.2:c.799-60_799-59delinsAT	NP_665809.1:n.799-60_799-59delinsAT
XM_011511957.1:c.955-60_955-59delinsAT	XP_011510259.1:n.955-60_955-59delinsAT
XR_923034.1:n.1934-60_1934-59delinsAT
NM_031942.5:c.1036-60_1036-59delinsAT MANE Select	NP_114148.3:n.1036-60_1036-59delinsAT
NM_145810.3:c.799-60_799-59delinsAT	NP_665809.1:n.799-60_799-59delinsAT