Canonical Allele Identifier: CA2661982996

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366255-G-GTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366260_173366263dup , CM000664.2:g.173366260_173366263dup	GRCh38
NC_000002.11:g.174230988_174230991dup , CM000664.1:g.174230988_174230991dup	GRCh37
NC_000002.10:g.173939234_173939237dup	NCBI36
NG_047202.1:g.17244_17247dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+668_798+671dup	ENSP00000512251.1:n.798+668_798+671dup
ENST00000695911.1:c.814-23_814-20dup	ENSP00000512262.1:n.814-23_814-20dup
ENST00000695912.1:c.1033-23_1033-20dup	ENSP00000512263.1:n.1033-23_1033-20dup
ENST00000695913.1:c.*1766_*1769dup	ENSP00000512264.1:n.*1766_*1769dup
ENST00000695914.1:c.796-23_796-20dup	ENSP00000512265.1:n.796-23_796-20dup
ENST00000695918.1:n.264-23_264-20dup
ENST00000306721.8:c.1036-23_1036-20dup MANE Select	ENSP00000306968.3:n.1036-23_1036-20dup
ENST00000306721.7:c.1036-23_1036-20dup	ENSP00000306968.3:n.1036-23_1036-20dup
ENST00000347703.7:c.799-23_799-20dup	ENSP00000272789.4:n.799-23_799-20dup
ENST00000410019.3:c.673-23_673-20dup	ENSP00000386833.3:n.673-23_673-20dup
ENST00000410101.7:c.904-23_904-20dup	ENSP00000386656.3:n.904-23_904-20dup
ENST00000467411.5:n.1768+668_1768+671dup
ENST00000496441.5:n.1790-23_1790-20dup
NM_031942.4:c.1036-23_1036-20dup	NP_114148.3:n.1036-23_1036-20dup
NM_145810.2:c.799-23_799-20dup	NP_665809.1:n.799-23_799-20dup
XM_011511957.1:c.955-23_955-20dup	XP_011510259.1:n.955-23_955-20dup
XR_923034.1:n.1934-23_1934-20dup
NM_031942.5:c.1036-23_1036-20dup MANE Select	NP_114148.3:n.1036-23_1036-20dup
NM_145810.3:c.799-23_799-20dup	NP_665809.1:n.799-23_799-20dup