Canonical Allele Identifier: CA1308216301

Gene: CDCA7

Linked Data

• dbSNP Id: rs1686713725

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366053_173366054del , CM000664.2:g.173366053_173366054del	GRCh38
NC_000002.11:g.174230781_174230782del , CM000664.1:g.174230781_174230782del	GRCh37
NC_000002.10:g.173939027_173939028del	NCBI36
NG_047202.1:g.17037_17038del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+461_798+462del	ENSP00000512251.1:n.798+461_798+462del
ENST00000695911.1:c.814-230_814-229del	ENSP00000512262.1:n.814-230_814-229del
ENST00000695912.1:c.1033-230_1033-229del	ENSP00000512263.1:n.1033-230_1033-229del
ENST00000695913.1:c.*1559_*1560del	ENSP00000512264.1:n.*1559_*1560del
ENST00000695914.1:c.796-230_796-229del	ENSP00000512265.1:n.796-230_796-229del
ENST00000695918.1:n.264-230_264-229del
ENST00000306721.8:c.1036-230_1036-229del MANE Select	ENSP00000306968.3:n.1036-230_1036-229del
ENST00000306721.7:c.1036-230_1036-229del	ENSP00000306968.3:n.1036-230_1036-229del
ENST00000347703.7:c.799-230_799-229del	ENSP00000272789.4:n.799-230_799-229del
ENST00000410019.3:c.673-230_673-229del	ENSP00000386833.3:n.673-230_673-229del
ENST00000410101.7:c.904-230_904-229del	ENSP00000386656.3:n.904-230_904-229del
ENST00000467411.5:n.1768+461_1768+462del
ENST00000496441.5:n.1790-230_1790-229del
NM_031942.4:c.1036-230_1036-229del	NP_114148.3:n.1036-230_1036-229del
NM_145810.2:c.799-230_799-229del	NP_665809.1:n.799-230_799-229del
XM_011511957.1:c.955-230_955-229del	XP_011510259.1:n.955-230_955-229del
XR_923034.1:n.1934-230_1934-229del
NM_031942.5:c.1036-230_1036-229del MANE Select	NP_114148.3:n.1036-230_1036-229del
NM_145810.3:c.799-230_799-229del	NP_665809.1:n.799-230_799-229del