Canonical Allele Identifier: CA2661982947

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366220-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366220G>T , CM000664.2:g.173366220G>T	GRCh38
NC_000002.11:g.174230948G>T , CM000664.1:g.174230948G>T	GRCh37
NC_000002.10:g.173939194G>T	NCBI36
NG_047202.1:g.17204G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+628G>T	ENSP00000512251.1:n.798+628G>T
ENST00000695911.1:c.814-63G>T	ENSP00000512262.1:n.814-63G>T
ENST00000695912.1:c.1033-63G>T	ENSP00000512263.1:n.1033-63G>T
ENST00000695913.1:c.*1726G>T	ENSP00000512264.1:n.*1726G>T
ENST00000695914.1:c.796-63G>T	ENSP00000512265.1:n.796-63G>T
ENST00000695918.1:n.264-63G>T
ENST00000306721.8:c.1036-63G>T MANE Select	ENSP00000306968.3:n.1036-63G>T
ENST00000306721.7:c.1036-63G>T	ENSP00000306968.3:n.1036-63G>T
ENST00000347703.7:c.799-63G>T	ENSP00000272789.4:n.799-63G>T
ENST00000410019.3:c.673-63G>T	ENSP00000386833.3:n.673-63G>T
ENST00000410101.7:c.904-63G>T	ENSP00000386656.3:n.904-63G>T
ENST00000467411.5:n.1768+628G>T
ENST00000496441.5:n.1790-63G>T
NM_031942.4:c.1036-63G>T	NP_114148.3:n.1036-63G>T
NM_145810.2:c.799-63G>T	NP_665809.1:n.799-63G>T
XM_011511957.1:c.955-63G>T	XP_011510259.1:n.955-63G>T
XR_923034.1:n.1934-63G>T
NM_031942.5:c.1036-63G>T MANE Select	NP_114148.3:n.1036-63G>T
NM_145810.3:c.799-63G>T	NP_665809.1:n.799-63G>T