Canonical Allele Identifier: CA760834584

Gene: CDCA7

Linked Data

• dbSNP Id: rs1168680423
• gnomAD v3: 2-173366032-C-G
• gnomAD v4: 2-173366032-C-G
• MyVariant Identifiers: chr2:g.174230760C>G (hg19) ; chr2:g.173366032C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366032C>G , CM000664.2:g.173366032C>G	GRCh38
NC_000002.11:g.174230760C>G , CM000664.1:g.174230760C>G	GRCh37
NC_000002.10:g.173939006C>G	NCBI36
NG_047202.1:g.17016C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+440C>G	ENSP00000512251.1:n.798+440C>G
ENST00000695911.1:c.814-251C>G	ENSP00000512262.1:n.814-251C>G
ENST00000695912.1:c.1033-251C>G	ENSP00000512263.1:n.1033-251C>G
ENST00000695913.1:c.*1538C>G	ENSP00000512264.1:n.*1538C>G
ENST00000695914.1:c.796-251C>G	ENSP00000512265.1:n.796-251C>G
ENST00000695918.1:n.264-251C>G
ENST00000306721.8:c.1036-251C>G MANE Select	ENSP00000306968.3:n.1036-251C>G
ENST00000306721.7:c.1036-251C>G	ENSP00000306968.3:n.1036-251C>G
ENST00000347703.7:c.799-251C>G	ENSP00000272789.4:n.799-251C>G
ENST00000410019.3:c.673-251C>G	ENSP00000386833.3:n.673-251C>G
ENST00000410101.7:c.904-251C>G	ENSP00000386656.3:n.904-251C>G
ENST00000467411.5:n.1768+440C>G
ENST00000496441.5:n.1790-251C>G
NM_031942.4:c.1036-251C>G	NP_114148.3:n.1036-251C>G
NM_145810.2:c.799-251C>G	NP_665809.1:n.799-251C>G
XM_011511957.1:c.955-251C>G	XP_011510259.1:n.955-251C>G
XR_923034.1:n.1934-251C>G
NM_031942.5:c.1036-251C>G MANE Select	NP_114148.3:n.1036-251C>G
NM_145810.3:c.799-251C>G	NP_665809.1:n.799-251C>G