Canonical Allele Identifier: CA2661982898

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366143-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366145del , CM000664.2:g.173366145del	GRCh38
NC_000002.11:g.174230873del , CM000664.1:g.174230873del	GRCh37
NC_000002.10:g.173939119del	NCBI36
NG_047202.1:g.17129del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+553del	ENSP00000512251.1:n.798+553del
ENST00000695911.1:c.814-138del	ENSP00000512262.1:n.814-138del
ENST00000695912.1:c.1033-138del	ENSP00000512263.1:n.1033-138del
ENST00000695913.1:c.*1651del	ENSP00000512264.1:n.*1651del
ENST00000695914.1:c.796-138del	ENSP00000512265.1:n.796-138del
ENST00000695918.1:n.264-138del
ENST00000306721.8:c.1036-138del MANE Select	ENSP00000306968.3:n.1036-138del
ENST00000306721.7:c.1036-138del	ENSP00000306968.3:n.1036-138del
ENST00000347703.7:c.799-138del	ENSP00000272789.4:n.799-138del
ENST00000410019.3:c.673-138del	ENSP00000386833.3:n.673-138del
ENST00000410101.7:c.904-138del	ENSP00000386656.3:n.904-138del
ENST00000467411.5:n.1768+553del
ENST00000496441.5:n.1790-138del
NM_031942.4:c.1036-138del	NP_114148.3:n.1036-138del
NM_145810.2:c.799-138del	NP_665809.1:n.799-138del
XM_011511957.1:c.955-138del	XP_011510259.1:n.955-138del
XR_923034.1:n.1934-138del
NM_031942.5:c.1036-138del MANE Select	NP_114148.3:n.1036-138del
NM_145810.3:c.799-138del	NP_665809.1:n.799-138del