Canonical Allele Identifier: CA2577162099

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366222-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366222C>A , CM000664.2:g.173366222C>A	GRCh38
NC_000002.11:g.174230950C>A , CM000664.1:g.174230950C>A	GRCh37
NC_000002.10:g.173939196C>A	NCBI36
NG_047202.1:g.17206C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+630C>A	ENSP00000512251.1:n.798+630C>A
ENST00000695911.1:c.814-61C>A	ENSP00000512262.1:n.814-61C>A
ENST00000695912.1:c.1033-61C>A	ENSP00000512263.1:n.1033-61C>A
ENST00000695913.1:c.*1728C>A	ENSP00000512264.1:n.*1728C>A
ENST00000695914.1:c.796-61C>A	ENSP00000512265.1:n.796-61C>A
ENST00000695918.1:n.264-61C>A
ENST00000306721.8:c.1036-61C>A MANE Select	ENSP00000306968.3:n.1036-61C>A
ENST00000306721.7:c.1036-61C>A	ENSP00000306968.3:n.1036-61C>A
ENST00000347703.7:c.799-61C>A	ENSP00000272789.4:n.799-61C>A
ENST00000410019.3:c.673-61C>A	ENSP00000386833.3:n.673-61C>A
ENST00000410101.7:c.904-61C>A	ENSP00000386656.3:n.904-61C>A
ENST00000467411.5:n.1768+630C>A
ENST00000496441.5:n.1790-61C>A
NM_031942.4:c.1036-61C>A	NP_114148.3:n.1036-61C>A
NM_145810.2:c.799-61C>A	NP_665809.1:n.799-61C>A
XM_011511957.1:c.955-61C>A	XP_011510259.1:n.955-61C>A
XR_923034.1:n.1934-61C>A
NM_031942.5:c.1036-61C>A MANE Select	NP_114148.3:n.1036-61C>A
NM_145810.3:c.799-61C>A	NP_665809.1:n.799-61C>A