Canonical Allele Identifier: CA1971437

Gene: CDCA7

Linked Data

• dbSNP Id: rs765556479
• ExAC: 2:174231051 C / G
• gnomAD v2: 2-174231051-C-G
• gnomAD v4: 2-173366323-C-G
• MyVariant Identifiers: chr2:g.174231051C>G (hg19) ; chr2:g.173366323C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+731C>G	ENSP00000512251.1:n.798+731C>G
ENST00000695911.1:c.854C>G	ENSP00000512262.1:n.854C>G
ENST00000695912.1:c.1073C>G	ENSP00000512263.1:p.Thr358Ser
ENST00000695913.1:c.*1829C>G	ENSP00000512264.1:n.*1829C>G
ENST00000695914.1:c.836C>G	ENSP00000512265.1:p.Thr279Ser
ENST00000695918.1:n.304C>G
ENST00000306721.8:c.1076C>G MANE Select	ENSP00000306968.3:p.Thr359Ser
ENST00000306721.7:c.1076C>G	ENSP00000306968.3:p.Thr359Ser
ENST00000347703.7:c.839C>G	ENSP00000272789.4:p.Thr280Ser
ENST00000410019.3:c.713C>G	ENSP00000386833.3:p.Thr238Ser
ENST00000410101.7:c.944C>G	ENSP00000386656.3:p.Thr315Ser
ENST00000467411.5:n.1768+731C>G
ENST00000496441.5:n.1830C>G
NM_031942.4:c.1076C>G	NP_114148.3:p.Thr359Ser
NM_145810.2:c.839C>G	NP_665809.1:p.Thr280Ser
XM_011511957.1:c.995C>G	XP_011510259.1:p.Thr332Ser
XR_923034.1:n.1974C>G
NM_031942.5:c.1076C>G MANE Select	NP_114148.3:p.Thr359Ser
NM_145810.3:c.839C>G	NP_665809.1:p.Thr280Ser