Canonical Allele Identifier: CA349330471

Gene: CDCA7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+722C>A	ENSP00000512251.1:n.798+722C>A
ENST00000695911.1:c.845C>A	ENSP00000512262.1:n.845C>A
ENST00000695912.1:c.1064C>A	ENSP00000512263.1:p.Thr355Asn
ENST00000695913.1:c.*1820C>A	ENSP00000512264.1:n.*1820C>A
ENST00000695914.1:c.827C>A	ENSP00000512265.1:p.Thr276Asn
ENST00000695918.1:n.295C>A
ENST00000306721.8:c.1067C>A MANE Select	ENSP00000306968.3:p.Thr356Asn
ENST00000306721.7:c.1067C>A	ENSP00000306968.3:p.Thr356Asn
ENST00000347703.7:c.830C>A	ENSP00000272789.4:p.Thr277Asn
ENST00000410019.3:c.704C>A	ENSP00000386833.3:p.Thr235Asn
ENST00000410101.7:c.935C>A	ENSP00000386656.3:p.Thr312Asn
ENST00000467411.5:n.1768+722C>A
ENST00000496441.5:n.1821C>A
NM_031942.4:c.1067C>A	NP_114148.3:p.Thr356Asn
NM_145810.2:c.830C>A	NP_665809.1:p.Thr277Asn
XM_011511957.1:c.986C>A	XP_011510259.1:p.Thr329Asn
XR_923034.1:n.1965C>A
NM_031942.5:c.1067C>A MANE Select	NP_114148.3:p.Thr356Asn
NM_145810.3:c.830C>A	NP_665809.1:p.Thr277Asn