Canonical Allele Identifier: CA349330561

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231060A>G (hg19) ; chr2:g.173366332A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366332A>G , CM000664.2:g.173366332A>G	GRCh38
NC_000002.11:g.174231060A>G , CM000664.1:g.174231060A>G	GRCh37
NC_000002.10:g.173939306A>G	NCBI36
NG_047202.1:g.17316A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+740A>G	ENSP00000512251.1:n.798+740A>G
ENST00000695911.1:c.863A>G	ENSP00000512262.1:n.863A>G
ENST00000695912.1:c.1082A>G	ENSP00000512263.1:p.Asn361Ser
ENST00000695913.1:c.*1838A>G	ENSP00000512264.1:n.*1838A>G
ENST00000695914.1:c.845A>G	ENSP00000512265.1:p.Asn282Ser
ENST00000695918.1:n.313A>G
ENST00000306721.8:c.1085A>G MANE Select	ENSP00000306968.3:p.Asn362Ser
ENST00000306721.7:c.1085A>G	ENSP00000306968.3:p.Asn362Ser
ENST00000347703.7:c.848A>G	ENSP00000272789.4:p.Asn283Ser
ENST00000410019.3:c.722A>G	ENSP00000386833.3:p.Asn241Ser
ENST00000410101.7:c.953A>G	ENSP00000386656.3:p.Asn318Ser
ENST00000467411.5:n.1768+740A>G
ENST00000496441.5:n.1839A>G
NM_031942.4:c.1085A>G	NP_114148.3:p.Asn362Ser
NM_145810.2:c.848A>G	NP_665809.1:p.Asn283Ser
XM_011511957.1:c.1004A>G	XP_011510259.1:p.Asn335Ser
XR_923034.1:n.1983A>G
NM_031942.5:c.1085A>G MANE Select	NP_114148.3:p.Asn362Ser
NM_145810.3:c.848A>G	NP_665809.1:p.Asn283Ser