Canonical Allele Identifier: CA349331004

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231142G>T (hg19) ; chr2:g.173366414G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366414G>T , CM000664.2:g.173366414G>T	GRCh38
NC_000002.11:g.174231142G>T , CM000664.1:g.174231142G>T	GRCh37
NC_000002.10:g.173939388G>T	NCBI36
NG_047202.1:g.17398G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-736G>T	ENSP00000512251.1:n.799-736G>T
ENST00000695911.1:c.945G>T	ENSP00000512262.1:n.945G>T
ENST00000695912.1:c.1164G>T	ENSP00000512263.1:p.Arg388Ser
ENST00000695913.1:c.*1920G>T	ENSP00000512264.1:n.*1920G>T
ENST00000695914.1:c.927G>T	ENSP00000512265.1:p.Arg309Ser
ENST00000695918.1:n.395G>T
ENST00000306721.8:c.1167G>T MANE Select	ENSP00000306968.3:p.Arg389Ser
ENST00000306721.7:c.1167G>T	ENSP00000306968.3:p.Arg389Ser
ENST00000347703.7:c.930G>T	ENSP00000272789.4:p.Arg310Ser
ENST00000410019.3:c.804G>T	ENSP00000386833.3:p.Arg268Ser
ENST00000410101.7:c.1035G>T	ENSP00000386656.3:p.Arg345Ser
ENST00000467411.5:n.1769-736G>T
ENST00000496441.5:n.1921G>T
NM_031942.4:c.1167G>T	NP_114148.3:p.Arg389Ser
NM_145810.2:c.930G>T	NP_665809.1:p.Arg310Ser
XM_011511957.1:c.1086G>T	XP_011510259.1:p.Arg362Ser
XR_923034.1:n.2065G>T
NM_031942.5:c.1167G>T MANE Select	NP_114148.3:p.Arg389Ser
NM_145810.3:c.930G>T	NP_665809.1:p.Arg310Ser