Canonical Allele Identifier: CA349330581

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231063G>C (hg19) ; chr2:g.173366335G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366335G>C , CM000664.2:g.173366335G>C	GRCh38
NC_000002.11:g.174231063G>C , CM000664.1:g.174231063G>C	GRCh37
NC_000002.10:g.173939309G>C	NCBI36
NG_047202.1:g.17319G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+743G>C	ENSP00000512251.1:n.798+743G>C
ENST00000695911.1:c.866G>C	ENSP00000512262.1:n.866G>C
ENST00000695912.1:c.1085G>C	ENSP00000512263.1:p.Cys362Ser
ENST00000695913.1:c.*1841G>C	ENSP00000512264.1:n.*1841G>C
ENST00000695914.1:c.848G>C	ENSP00000512265.1:p.Cys283Ser
ENST00000695918.1:n.316G>C
ENST00000306721.8:c.1088G>C MANE Select	ENSP00000306968.3:p.Cys363Ser
ENST00000306721.7:c.1088G>C	ENSP00000306968.3:p.Cys363Ser
ENST00000347703.7:c.851G>C	ENSP00000272789.4:p.Cys284Ser
ENST00000410019.3:c.725G>C	ENSP00000386833.3:p.Cys242Ser
ENST00000410101.7:c.956G>C	ENSP00000386656.3:p.Cys319Ser
ENST00000467411.5:n.1768+743G>C
ENST00000496441.5:n.1842G>C
NM_031942.4:c.1088G>C	NP_114148.3:p.Cys363Ser
NM_145810.2:c.851G>C	NP_665809.1:p.Cys284Ser
XM_011511957.1:c.1007G>C	XP_011510259.1:p.Cys336Ser
XR_923034.1:n.1986G>C
NM_031942.5:c.1088G>C MANE Select	NP_114148.3:p.Cys363Ser
NM_145810.3:c.851G>C	NP_665809.1:p.Cys284Ser