Canonical Allele Identifier: CA349330472

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231042C>T (hg19) ; chr2:g.173366314C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366314C>T , CM000664.2:g.173366314C>T	GRCh38
NC_000002.11:g.174231042C>T , CM000664.1:g.174231042C>T	GRCh37
NC_000002.10:g.173939288C>T	NCBI36
NG_047202.1:g.17298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+722C>T	ENSP00000512251.1:n.798+722C>T
ENST00000695911.1:c.845C>T	ENSP00000512262.1:n.845C>T
ENST00000695912.1:c.1064C>T	ENSP00000512263.1:p.Thr355Ile
ENST00000695913.1:c.*1820C>T	ENSP00000512264.1:n.*1820C>T
ENST00000695914.1:c.827C>T	ENSP00000512265.1:p.Thr276Ile
ENST00000695918.1:n.295C>T
ENST00000306721.8:c.1067C>T MANE Select	ENSP00000306968.3:p.Thr356Ile
ENST00000306721.7:c.1067C>T	ENSP00000306968.3:p.Thr356Ile
ENST00000347703.7:c.830C>T	ENSP00000272789.4:p.Thr277Ile
ENST00000410019.3:c.704C>T	ENSP00000386833.3:p.Thr235Ile
ENST00000410101.7:c.935C>T	ENSP00000386656.3:p.Thr312Ile
ENST00000467411.5:n.1768+722C>T
ENST00000496441.5:n.1821C>T
NM_031942.4:c.1067C>T	NP_114148.3:p.Thr356Ile
NM_145810.2:c.830C>T	NP_665809.1:p.Thr277Ile
XM_011511957.1:c.986C>T	XP_011510259.1:p.Thr329Ile
XR_923034.1:n.1965C>T
NM_031942.5:c.1067C>T MANE Select	NP_114148.3:p.Thr356Ile
NM_145810.3:c.830C>T	NP_665809.1:p.Thr277Ile