Canonical Allele Identifier: CA349330423

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231031C>A (hg19) ; chr2:g.173366303C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366303C>A , CM000664.2:g.173366303C>A	GRCh38
NC_000002.11:g.174231031C>A , CM000664.1:g.174231031C>A	GRCh37
NC_000002.10:g.173939277C>A	NCBI36
NG_047202.1:g.17287C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+711C>A	ENSP00000512251.1:n.798+711C>A
ENST00000695911.1:c.834C>A	ENSP00000512262.1:n.834C>A
ENST00000695912.1:c.1053C>A	ENSP00000512263.1:p.Cys351Ter
ENST00000695913.1:c.*1809C>A	ENSP00000512264.1:n.*1809C>A
ENST00000695914.1:c.816C>A	ENSP00000512265.1:p.Cys272Ter
ENST00000695918.1:n.284C>A
ENST00000306721.8:c.1056C>A MANE Select	ENSP00000306968.3:p.Cys352Ter
ENST00000306721.7:c.1056C>A	ENSP00000306968.3:p.Cys352Ter
ENST00000347703.7:c.819C>A	ENSP00000272789.4:p.Cys273Ter
ENST00000410019.3:c.693C>A	ENSP00000386833.3:p.Cys231Ter
ENST00000410101.7:c.924C>A	ENSP00000386656.3:p.Cys308Ter
ENST00000467411.5:n.1768+711C>A
ENST00000496441.5:n.1810C>A
NM_031942.4:c.1056C>A	NP_114148.3:p.Cys352Ter
NM_145810.2:c.819C>A	NP_665809.1:p.Cys273Ter
XM_011511957.1:c.975C>A	XP_011510259.1:p.Cys325Ter
XR_923034.1:n.1954C>A
NM_031942.5:c.1056C>A MANE Select	NP_114148.3:p.Cys352Ter
NM_145810.3:c.819C>A	NP_665809.1:p.Cys273Ter