Canonical Allele Identifier: CA60779796

Gene: CDCA7

Linked Data

• dbSNP Id: rs916154256
• MyVariant Identifiers: chr2:g.174230743G>C (hg19) ; chr2:g.173366015G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366015G>C , CM000664.2:g.173366015G>C	GRCh38
NC_000002.11:g.174230743G>C , CM000664.1:g.174230743G>C	GRCh37
NC_000002.10:g.173938989G>C	NCBI36
NG_047202.1:g.16999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+423G>C	ENSP00000512251.1:n.798+423G>C
ENST00000695911.1:c.814-268G>C	ENSP00000512262.1:n.814-268G>C
ENST00000695912.1:c.1033-268G>C	ENSP00000512263.1:n.1033-268G>C
ENST00000695913.1:c.*1521G>C	ENSP00000512264.1:n.*1521G>C
ENST00000695914.1:c.796-268G>C	ENSP00000512265.1:n.796-268G>C
ENST00000695918.1:n.264-268G>C
ENST00000306721.8:c.1036-268G>C MANE Select	ENSP00000306968.3:n.1036-268G>C
ENST00000306721.7:c.1036-268G>C	ENSP00000306968.3:n.1036-268G>C
ENST00000347703.7:c.799-268G>C	ENSP00000272789.4:n.799-268G>C
ENST00000410019.3:c.673-268G>C	ENSP00000386833.3:n.673-268G>C
ENST00000410101.7:c.904-268G>C	ENSP00000386656.3:n.904-268G>C
ENST00000467411.5:n.1768+423G>C
ENST00000496441.5:n.1790-268G>C
NM_031942.4:c.1036-268G>C	NP_114148.3:n.1036-268G>C
NM_145810.2:c.799-268G>C	NP_665809.1:n.799-268G>C
XM_011511957.1:c.955-268G>C	XP_011510259.1:n.955-268G>C
XR_923034.1:n.1934-268G>C
NM_031942.5:c.1036-268G>C MANE Select	NP_114148.3:n.1036-268G>C
NM_145810.3:c.799-268G>C	NP_665809.1:n.799-268G>C