Canonical Allele Identifier: CA429810477

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231058A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366330A>T , CM000664.2:g.173366330A>T	GRCh38
NC_000002.11:g.174231058A>T , CM000664.1:g.174231058A>T	GRCh37
NC_000002.10:g.173939304A>T	NCBI36
NG_047202.1:g.17314A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+738A>T	ENSP00000512251.1:n.798+738A>T
ENST00000695911.1:c.861A>T	ENSP00000512262.1:n.861A>T
ENST00000695912.1:c.1080A>T	ENSP00000512263.1:p.Thr360=
ENST00000695913.1:c.*1836A>T	ENSP00000512264.1:n.*1836A>T
ENST00000695914.1:c.843A>T	ENSP00000512265.1:p.Thr281=
ENST00000695918.1:n.311A>T
ENST00000306721.8:c.1083A>T MANE Select	ENSP00000306968.3:p.Thr361=
ENST00000306721.7:c.1083A>T	ENSP00000306968.3:p.Thr361=
ENST00000347703.7:c.846A>T	ENSP00000272789.4:p.Thr282=
ENST00000410019.3:c.720A>T	ENSP00000386833.3:p.Thr240=
ENST00000410101.7:c.951A>T	ENSP00000386656.3:p.Thr317=
ENST00000467411.5:n.1768+738A>T
ENST00000496441.5:n.1837A>T
NM_031942.4:c.1083A>T	NP_114148.3:p.Thr361=
NM_145810.2:c.846A>T	NP_665809.1:p.Thr282=
XM_011511957.1:c.1002A>T	XP_011510259.1:p.Thr334=
XR_923034.1:n.1981A>T
NM_031942.5:c.1083A>T MANE Select	NP_114148.3:p.Thr361=
NM_145810.3:c.846A>T	NP_665809.1:p.Thr282=