Canonical Allele Identifier: CA1308216284

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366013_173366014delinsTG , CM000664.2:g.173366013_173366014delinsTG	GRCh38
NC_000002.11:g.174230741_174230742delinsTG , CM000664.1:g.174230741_174230742delinsTG	GRCh37
NC_000002.10:g.173938987_173938988delinsTG	NCBI36
NG_047202.1:g.16997_16998delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+421_798+422delinsTG	ENSP00000512251.1:n.798+421_798+422delinsTG
ENST00000695911.1:c.814-270_814-269delinsTG	ENSP00000512262.1:n.814-270_814-269delinsTG
ENST00000695912.1:c.1033-270_1033-269delinsTG	ENSP00000512263.1:n.1033-270_1033-269delinsTG
ENST00000695913.1:c.*1519_*1520delinsTG	ENSP00000512264.1:n.*1519_*1520delinsTG
ENST00000695914.1:c.796-270_796-269delinsTG	ENSP00000512265.1:n.796-270_796-269delinsTG
ENST00000695918.1:n.264-270_264-269delinsTG
ENST00000306721.8:c.1036-270_1036-269delinsTG MANE Select	ENSP00000306968.3:n.1036-270_1036-269delinsTG
ENST00000306721.7:c.1036-270_1036-269delinsTG	ENSP00000306968.3:n.1036-270_1036-269delinsTG
ENST00000347703.7:c.799-270_799-269delinsTG	ENSP00000272789.4:n.799-270_799-269delinsTG
ENST00000410019.3:c.673-270_673-269delinsTG	ENSP00000386833.3:n.673-270_673-269delinsTG
ENST00000410101.7:c.904-270_904-269delinsTG	ENSP00000386656.3:n.904-270_904-269delinsTG
ENST00000467411.5:n.1768+421_1768+422delinsTG
ENST00000496441.5:n.1790-270_1790-269delinsTG
NM_031942.4:c.1036-270_1036-269delinsTG	NP_114148.3:n.1036-270_1036-269delinsTG
NM_145810.2:c.799-270_799-269delinsTG	NP_665809.1:n.799-270_799-269delinsTG
XM_011511957.1:c.955-270_955-269delinsTG	XP_011510259.1:n.955-270_955-269delinsTG
XR_923034.1:n.1934-270_1934-269delinsTG
NM_031942.5:c.1036-270_1036-269delinsTG MANE Select	NP_114148.3:n.1036-270_1036-269delinsTG
NM_145810.3:c.799-270_799-269delinsTG	NP_665809.1:n.799-270_799-269delinsTG