Canonical Allele Identifier: CA537974561

Gene: CDCA7

Linked Data

• dbSNP Id: rs1274559896
• gnomAD v2: 2-174230997-TGGC-T
• gnomAD v4: 2-173366269-TGGC-T
• MyVariant Identifiers: chr2:g.174230998_174231000del (hg19) ; chr2:g.173366270_173366272del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366270_173366272del , CM000664.2:g.173366270_173366272del	GRCh38
NC_000002.11:g.174230998_174231000del , CM000664.1:g.174230998_174231000del	GRCh37
NC_000002.10:g.173939244_173939246del	NCBI36
NG_047202.1:g.17254_17256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+678_798+680del	ENSP00000512251.1:n.798+678_798+680del
ENST00000695911.1:c.814-13_814-11del	ENSP00000512262.1:n.814-13_814-11del
ENST00000695912.1:c.1033-13_1033-11del	ENSP00000512263.1:n.1033-13_1033-11del
ENST00000695913.1:c.*1776_*1778del	ENSP00000512264.1:n.*1776_*1778del
ENST00000695914.1:c.796-13_796-11del	ENSP00000512265.1:n.796-13_796-11del
ENST00000695918.1:n.264-13_264-11del
ENST00000306721.8:c.1036-13_1036-11del MANE Select	ENSP00000306968.3:n.1036-13_1036-11del
ENST00000306721.7:c.1036-13_1036-11del	ENSP00000306968.3:n.1036-13_1036-11del
ENST00000347703.7:c.799-13_799-11del	ENSP00000272789.4:n.799-13_799-11del
ENST00000410019.3:c.673-13_673-11del	ENSP00000386833.3:n.673-13_673-11del
ENST00000410101.7:c.904-13_904-11del	ENSP00000386656.3:n.904-13_904-11del
ENST00000467411.5:n.1768+678_1768+680del
ENST00000496441.5:n.1790-13_1790-11del
NM_031942.4:c.1036-13_1036-11del	NP_114148.3:n.1036-13_1036-11del
NM_145810.2:c.799-13_799-11del	NP_665809.1:n.799-13_799-11del
XM_011511957.1:c.955-13_955-11del	XP_011510259.1:n.955-13_955-11del
XR_923034.1:n.1934-13_1934-11del
NM_031942.5:c.1036-13_1036-11del MANE Select	NP_114148.3:n.1036-13_1036-11del
NM_145810.3:c.799-13_799-11del	NP_665809.1:n.799-13_799-11del