Canonical Allele Identifier: CA1308216322

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366113_173366115delinsCTG , CM000664.2:g.173366113_173366115delinsCTG	GRCh38
NC_000002.11:g.174230841_174230843delinsCTG , CM000664.1:g.174230841_174230843delinsCTG	GRCh37
NC_000002.10:g.173939087_173939089delinsCTG	NCBI36
NG_047202.1:g.17097_17099delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+521_798+523delinsCTG	ENSP00000512251.1:n.798+521_798+523delinsCTG
ENST00000695911.1:c.814-170_814-168delinsCTG	ENSP00000512262.1:n.814-170_814-168delinsCTG
ENST00000695912.1:c.1033-170_1033-168delinsCTG	ENSP00000512263.1:n.1033-170_1033-168delinsCTG
ENST00000695913.1:c.*1619_*1621delinsCTG	ENSP00000512264.1:n.*1619_*1621delinsCTG
ENST00000695914.1:c.796-170_796-168delinsCTG	ENSP00000512265.1:n.796-170_796-168delinsCTG
ENST00000695918.1:n.264-170_264-168delinsCTG
ENST00000306721.8:c.1036-170_1036-168delinsCTG MANE Select	ENSP00000306968.3:n.1036-170_1036-168delinsCTG
ENST00000306721.7:c.1036-170_1036-168delinsCTG	ENSP00000306968.3:n.1036-170_1036-168delinsCTG
ENST00000347703.7:c.799-170_799-168delinsCTG	ENSP00000272789.4:n.799-170_799-168delinsCTG
ENST00000410019.3:c.673-170_673-168delinsCTG	ENSP00000386833.3:n.673-170_673-168delinsCTG
ENST00000410101.7:c.904-170_904-168delinsCTG	ENSP00000386656.3:n.904-170_904-168delinsCTG
ENST00000467411.5:n.1768+521_1768+523delinsCTG
ENST00000496441.5:n.1790-170_1790-168delinsCTG
NM_031942.4:c.1036-170_1036-168delinsCTG	NP_114148.3:n.1036-170_1036-168delinsCTG
NM_145810.2:c.799-170_799-168delinsCTG	NP_665809.1:n.799-170_799-168delinsCTG
XM_011511957.1:c.955-170_955-168delinsCTG	XP_011510259.1:n.955-170_955-168delinsCTG
XR_923034.1:n.1934-170_1934-168delinsCTG
NM_031942.5:c.1036-170_1036-168delinsCTG MANE Select	NP_114148.3:n.1036-170_1036-168delinsCTG
NM_145810.3:c.799-170_799-168delinsCTG	NP_665809.1:n.799-170_799-168delinsCTG