Canonical Allele Identifier: CA1308216300

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366052_173366054delinsTTG , CM000664.2:g.173366052_173366054delinsTTG	GRCh38
NC_000002.11:g.174230780_174230782delinsTTG , CM000664.1:g.174230780_174230782delinsTTG	GRCh37
NC_000002.10:g.173939026_173939028delinsTTG	NCBI36
NG_047202.1:g.17036_17038delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+460_798+462delinsTTG	ENSP00000512251.1:n.798+460_798+462delinsTTG
ENST00000695911.1:c.814-231_814-229delinsTTG	ENSP00000512262.1:n.814-231_814-229delinsTTG
ENST00000695912.1:c.1033-231_1033-229delinsTTG	ENSP00000512263.1:n.1033-231_1033-229delinsTTG
ENST00000695913.1:c.*1558_*1560delinsTTG	ENSP00000512264.1:n.*1558_*1560delinsTTG
ENST00000695914.1:c.796-231_796-229delinsTTG	ENSP00000512265.1:n.796-231_796-229delinsTTG
ENST00000695918.1:n.264-231_264-229delinsTTG
ENST00000306721.8:c.1036-231_1036-229delinsTTG MANE Select	ENSP00000306968.3:n.1036-231_1036-229delinsTTG
ENST00000306721.7:c.1036-231_1036-229delinsTTG	ENSP00000306968.3:n.1036-231_1036-229delinsTTG
ENST00000347703.7:c.799-231_799-229delinsTTG	ENSP00000272789.4:n.799-231_799-229delinsTTG
ENST00000410019.3:c.673-231_673-229delinsTTG	ENSP00000386833.3:n.673-231_673-229delinsTTG
ENST00000410101.7:c.904-231_904-229delinsTTG	ENSP00000386656.3:n.904-231_904-229delinsTTG
ENST00000467411.5:n.1768+460_1768+462delinsTTG
ENST00000496441.5:n.1790-231_1790-229delinsTTG
NM_031942.4:c.1036-231_1036-229delinsTTG	NP_114148.3:n.1036-231_1036-229delinsTTG
NM_145810.2:c.799-231_799-229delinsTTG	NP_665809.1:n.799-231_799-229delinsTTG
XM_011511957.1:c.955-231_955-229delinsTTG	XP_011510259.1:n.955-231_955-229delinsTTG
XR_923034.1:n.1934-231_1934-229delinsTTG
NM_031942.5:c.1036-231_1036-229delinsTTG MANE Select	NP_114148.3:n.1036-231_1036-229delinsTTG
NM_145810.3:c.799-231_799-229delinsTTG	NP_665809.1:n.799-231_799-229delinsTTG