Canonical Allele Identifier: CA349330511

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231051C>A (hg19) ; chr2:g.173366323C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366323C>A , CM000664.2:g.173366323C>A	GRCh38
NC_000002.11:g.174231051C>A , CM000664.1:g.174231051C>A	GRCh37
NC_000002.10:g.173939297C>A	NCBI36
NG_047202.1:g.17307C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+731C>A	ENSP00000512251.1:n.798+731C>A
ENST00000695911.1:c.854C>A	ENSP00000512262.1:n.854C>A
ENST00000695912.1:c.1073C>A	ENSP00000512263.1:p.Thr358Asn
ENST00000695913.1:c.*1829C>A	ENSP00000512264.1:n.*1829C>A
ENST00000695914.1:c.836C>A	ENSP00000512265.1:p.Thr279Asn
ENST00000695918.1:n.304C>A
ENST00000306721.8:c.1076C>A MANE Select	ENSP00000306968.3:p.Thr359Asn
ENST00000306721.7:c.1076C>A	ENSP00000306968.3:p.Thr359Asn
ENST00000347703.7:c.839C>A	ENSP00000272789.4:p.Thr280Asn
ENST00000410019.3:c.713C>A	ENSP00000386833.3:p.Thr238Asn
ENST00000410101.7:c.944C>A	ENSP00000386656.3:p.Thr315Asn
ENST00000467411.5:n.1768+731C>A
ENST00000496441.5:n.1830C>A
NM_031942.4:c.1076C>A	NP_114148.3:p.Thr359Asn
NM_145810.2:c.839C>A	NP_665809.1:p.Thr280Asn
XM_011511957.1:c.995C>A	XP_011510259.1:p.Thr332Asn
XR_923034.1:n.1974C>A
NM_031942.5:c.1076C>A MANE Select	NP_114148.3:p.Thr359Asn
NM_145810.3:c.839C>A	NP_665809.1:p.Thr280Asn