Canonical Allele Identifier: CA760834646

Gene: CDCA7

Linked Data

• dbSNP Id: rs1266360965
• gnomAD v4: 2-173366187-CCTATA-C
• MyVariant Identifiers: chr2:g.174230916_174230920del (hg19) ; chr2:g.173366188_173366192del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366191_173366195del , CM000664.2:g.173366191_173366195del	GRCh38
NC_000002.11:g.174230919_174230923del , CM000664.1:g.174230919_174230923del	GRCh37
NC_000002.10:g.173939165_173939169del	NCBI36
NG_047202.1:g.17175_17179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+599_798+603del	ENSP00000512251.1:n.798+599_798+603del
ENST00000695911.1:c.814-92_814-88del	ENSP00000512262.1:n.814-92_814-88del
ENST00000695912.1:c.1033-92_1033-88del	ENSP00000512263.1:n.1033-92_1033-88del
ENST00000695913.1:c.*1697_*1701del	ENSP00000512264.1:n.*1697_*1701del
ENST00000695914.1:c.796-92_796-88del	ENSP00000512265.1:n.796-92_796-88del
ENST00000695918.1:n.264-92_264-88del
ENST00000306721.8:c.1036-92_1036-88del MANE Select	ENSP00000306968.3:n.1036-92_1036-88del
ENST00000306721.7:c.1036-92_1036-88del	ENSP00000306968.3:n.1036-92_1036-88del
ENST00000347703.7:c.799-92_799-88del	ENSP00000272789.4:n.799-92_799-88del
ENST00000410019.3:c.673-92_673-88del	ENSP00000386833.3:n.673-92_673-88del
ENST00000410101.7:c.904-92_904-88del	ENSP00000386656.3:n.904-92_904-88del
ENST00000467411.5:n.1768+599_1768+603del
ENST00000496441.5:n.1790-92_1790-88del
NM_031942.4:c.1036-92_1036-88del	NP_114148.3:n.1036-92_1036-88del
NM_145810.2:c.799-92_799-88del	NP_665809.1:n.799-92_799-88del
XM_011511957.1:c.955-92_955-88del	XP_011510259.1:n.955-92_955-88del
XR_923034.1:n.1934-92_1934-88del
NM_031942.5:c.1036-92_1036-88del MANE Select	NP_114148.3:n.1036-92_1036-88del
NM_145810.3:c.799-92_799-88del	NP_665809.1:n.799-92_799-88del