Canonical Allele Identifier: CA60780031

Gene: CDCA7

Linked Data

• dbSNP Id: rs796590246
• MyVariant Identifiers: chr2:g.174231074G>A (hg19) ; chr2:g.173366346G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366346G>A , CM000664.2:g.173366346G>A	GRCh38
NC_000002.11:g.174231074G>A , CM000664.1:g.174231074G>A	GRCh37
NC_000002.10:g.173939320G>A	NCBI36
NG_047202.1:g.17330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+754G>A	ENSP00000512251.1:n.798+754G>A
ENST00000695911.1:c.877G>A	ENSP00000512262.1:n.877G>A
ENST00000695912.1:c.1096G>A	ENSP00000512263.1:p.Asp366Asn
ENST00000695913.1:c.*1852G>A	ENSP00000512264.1:n.*1852G>A
ENST00000695914.1:c.859G>A	ENSP00000512265.1:p.Asp287Asn
ENST00000695918.1:n.327G>A
ENST00000306721.8:c.1099G>A MANE Select	ENSP00000306968.3:p.Asp367Asn
ENST00000306721.7:c.1099G>A	ENSP00000306968.3:p.Asp367Asn
ENST00000347703.7:c.862G>A	ENSP00000272789.4:p.Asp288Asn
ENST00000410019.3:c.736G>A	ENSP00000386833.3:p.Asp246Asn
ENST00000410101.7:c.967G>A	ENSP00000386656.3:p.Asp323Asn
ENST00000467411.5:n.1768+754G>A
ENST00000496441.5:n.1853G>A
NM_031942.4:c.1099G>A	NP_114148.3:p.Asp367Asn
NM_145810.2:c.862G>A	NP_665809.1:p.Asp288Asn
XM_011511957.1:c.1018G>A	XP_011510259.1:p.Asp340Asn
XR_923034.1:n.1997G>A
NM_031942.5:c.1099G>A MANE Select	NP_114148.3:p.Asp367Asn
NM_145810.3:c.862G>A	NP_665809.1:p.Asp288Asn