Canonical Allele Identifier: CA349330535

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231056A>C (hg19) ; chr2:g.173366328A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366328A>C , CM000664.2:g.173366328A>C	GRCh38
NC_000002.11:g.174231056A>C , CM000664.1:g.174231056A>C	GRCh37
NC_000002.10:g.173939302A>C	NCBI36
NG_047202.1:g.17312A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+736A>C	ENSP00000512251.1:n.798+736A>C
ENST00000695911.1:c.859A>C	ENSP00000512262.1:n.859A>C
ENST00000695912.1:c.1078A>C	ENSP00000512263.1:p.Thr360Pro
ENST00000695913.1:c.*1834A>C	ENSP00000512264.1:n.*1834A>C
ENST00000695914.1:c.841A>C	ENSP00000512265.1:p.Thr281Pro
ENST00000695918.1:n.309A>C
ENST00000306721.8:c.1081A>C MANE Select	ENSP00000306968.3:p.Thr361Pro
ENST00000306721.7:c.1081A>C	ENSP00000306968.3:p.Thr361Pro
ENST00000347703.7:c.844A>C	ENSP00000272789.4:p.Thr282Pro
ENST00000410019.3:c.718A>C	ENSP00000386833.3:p.Thr240Pro
ENST00000410101.7:c.949A>C	ENSP00000386656.3:p.Thr317Pro
ENST00000467411.5:n.1768+736A>C
ENST00000496441.5:n.1835A>C
NM_031942.4:c.1081A>C	NP_114148.3:p.Thr361Pro
NM_145810.2:c.844A>C	NP_665809.1:p.Thr282Pro
XM_011511957.1:c.1000A>C	XP_011510259.1:p.Thr334Pro
XR_923034.1:n.1979A>C
NM_031942.5:c.1081A>C MANE Select	NP_114148.3:p.Thr361Pro
NM_145810.3:c.844A>C	NP_665809.1:p.Thr282Pro