Canonical Allele Identifier: CA1971428

Gene: CDCA7

Linked Data

• dbSNP Id: rs773969240
• ExAC: 2:174230984 T / TC
• gnomAD v2: 2-174230984-T-TC
• gnomAD v4: 2-173366256-T-TC
• MyVariant Identifiers: chr2:g.174230984_174230985insC (hg19) ; chr2:g.173366256_173366257insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366256_173366257insC , CM000664.2:g.173366256_173366257insC	GRCh38
NC_000002.11:g.174230984_174230985insC , CM000664.1:g.174230984_174230985insC	GRCh37
NC_000002.10:g.173939230_173939231insC	NCBI36
NG_047202.1:g.17240_17241insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+664_798+665insC	ENSP00000512251.1:n.798+664_798+665insC
ENST00000695911.1:c.814-27_814-26insC	ENSP00000512262.1:n.814-27_814-26insC
ENST00000695912.1:c.1033-27_1033-26insC	ENSP00000512263.1:n.1033-27_1033-26insC
ENST00000695913.1:c.*1762_*1763insC	ENSP00000512264.1:n.*1762_*1763insC
ENST00000695914.1:c.796-27_796-26insC	ENSP00000512265.1:n.796-27_796-26insC
ENST00000695918.1:n.264-27_264-26insC
ENST00000306721.8:c.1036-27_1036-26insC MANE Select	ENSP00000306968.3:n.1036-27_1036-26insC
ENST00000306721.7:c.1036-27_1036-26insC	ENSP00000306968.3:n.1036-27_1036-26insC
ENST00000347703.7:c.799-27_799-26insC	ENSP00000272789.4:n.799-27_799-26insC
ENST00000410019.3:c.673-27_673-26insC	ENSP00000386833.3:n.673-27_673-26insC
ENST00000410101.7:c.904-27_904-26insC	ENSP00000386656.3:n.904-27_904-26insC
ENST00000467411.5:n.1768+664_1768+665insC
ENST00000496441.5:n.1790-27_1790-26insC
NM_031942.4:c.1036-27_1036-26insC	NP_114148.3:n.1036-27_1036-26insC
NM_145810.2:c.799-27_799-26insC	NP_665809.1:n.799-27_799-26insC
XM_011511957.1:c.955-27_955-26insC	XP_011510259.1:n.955-27_955-26insC
XR_923034.1:n.1934-27_1934-26insC
NM_031942.5:c.1036-27_1036-26insC MANE Select	NP_114148.3:n.1036-27_1036-26insC
NM_145810.3:c.799-27_799-26insC	NP_665809.1:n.799-27_799-26insC