Canonical Allele Identifier: CA60779818

Gene: CDCA7

Linked Data

• dbSNP Id: rs538258666
• gnomAD v2: 2-174230779-C-A
• gnomAD v3: 2-173366051-C-A
• gnomAD v4: 2-173366051-C-A
• MyVariant Identifiers: chr2:g.174230779C>A (hg19) ; chr2:g.173366051C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366051C>A , CM000664.2:g.173366051C>A	GRCh38
NC_000002.11:g.174230779C>A , CM000664.1:g.174230779C>A	GRCh37
NC_000002.10:g.173939025C>A	NCBI36
NG_047202.1:g.17035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+459C>A	ENSP00000512251.1:n.798+459C>A
ENST00000695911.1:c.814-232C>A	ENSP00000512262.1:n.814-232C>A
ENST00000695912.1:c.1033-232C>A	ENSP00000512263.1:n.1033-232C>A
ENST00000695913.1:c.*1557C>A	ENSP00000512264.1:n.*1557C>A
ENST00000695914.1:c.796-232C>A	ENSP00000512265.1:n.796-232C>A
ENST00000695918.1:n.264-232C>A
ENST00000306721.8:c.1036-232C>A MANE Select	ENSP00000306968.3:n.1036-232C>A
ENST00000306721.7:c.1036-232C>A	ENSP00000306968.3:n.1036-232C>A
ENST00000347703.7:c.799-232C>A	ENSP00000272789.4:n.799-232C>A
ENST00000410019.3:c.673-232C>A	ENSP00000386833.3:n.673-232C>A
ENST00000410101.7:c.904-232C>A	ENSP00000386656.3:n.904-232C>A
ENST00000467411.5:n.1768+459C>A
ENST00000496441.5:n.1790-232C>A
NM_031942.4:c.1036-232C>A	NP_114148.3:n.1036-232C>A
NM_145810.2:c.799-232C>A	NP_665809.1:n.799-232C>A
XM_011511957.1:c.955-232C>A	XP_011510259.1:n.955-232C>A
XR_923034.1:n.1934-232C>A
NM_031942.5:c.1036-232C>A MANE Select	NP_114148.3:n.1036-232C>A
NM_145810.3:c.799-232C>A	NP_665809.1:n.799-232C>A