Canonical Allele Identifier: CA1308216433

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366363_173366364delinsAG , CM000664.2:g.173366363_173366364delinsAG	GRCh38
NC_000002.11:g.174231091_174231092delinsAG , CM000664.1:g.174231091_174231092delinsAG	GRCh37
NC_000002.10:g.173939337_173939338delinsAG	NCBI36
NG_047202.1:g.17347_17348delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+771_798+772delinsAG	ENSP00000512251.1:n.798+771_798+772delinsAG
ENST00000695911.1:c.894_895delinsAG	ENSP00000512262.1:n.894_895delinsAG
ENST00000695912.1:c.1113_1114delinsAG	ENSP00000512263.1:p.Arg371=
ENST00000695913.1:c.*1869_*1870delinsAG	ENSP00000512264.1:n.*1869_*1870delinsAG
ENST00000695914.1:c.876_877delinsAG	ENSP00000512265.1:p.Arg292=
ENST00000695918.1:n.344_345delinsAG
ENST00000306721.8:c.1116_1117delinsAG MANE Select	ENSP00000306968.3:p.Arg372=
ENST00000306721.7:c.1116_1117delinsAG	ENSP00000306968.3:p.Arg372=
ENST00000347703.7:c.879_880delinsAG	ENSP00000272789.4:p.Arg293=
ENST00000410019.3:c.753_754delinsAG	ENSP00000386833.3:p.Arg251=
ENST00000410101.7:c.984_985delinsAG	ENSP00000386656.3:p.Arg328=
ENST00000467411.5:n.1768+771_1768+772delinsAG
ENST00000496441.5:n.1870_1871delinsAG
NM_031942.4:c.1116_1117delinsAG	NP_114148.3:p.Arg372=
NM_145810.2:c.879_880delinsAG	NP_665809.1:p.Arg293=
XM_011511957.1:c.1035_1036delinsAG	XP_011510259.1:p.Arg345=
XR_923034.1:n.2014_2015delinsAG
NM_031942.5:c.1116_1117delinsAG MANE Select	NP_114148.3:p.Arg372=
NM_145810.3:c.879_880delinsAG	NP_665809.1:p.Arg293=