Canonical Allele Identifier: CA349330779

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231099T>G (hg19) ; chr2:g.173366371T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366371T>G , CM000664.2:g.173366371T>G	GRCh38
NC_000002.11:g.174231099T>G , CM000664.1:g.174231099T>G	GRCh37
NC_000002.10:g.173939345T>G	NCBI36
NG_047202.1:g.17355T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-779T>G	ENSP00000512251.1:n.799-779T>G
ENST00000695911.1:c.902T>G	ENSP00000512262.1:n.902T>G
ENST00000695912.1:c.1121T>G	ENSP00000512263.1:p.Phe374Cys
ENST00000695913.1:c.*1877T>G	ENSP00000512264.1:n.*1877T>G
ENST00000695914.1:c.884T>G	ENSP00000512265.1:p.Phe295Cys
ENST00000695918.1:n.352T>G
ENST00000306721.8:c.1124T>G MANE Select	ENSP00000306968.3:p.Phe375Cys
ENST00000306721.7:c.1124T>G	ENSP00000306968.3:p.Phe375Cys
ENST00000347703.7:c.887T>G	ENSP00000272789.4:p.Phe296Cys
ENST00000410019.3:c.761T>G	ENSP00000386833.3:p.Phe254Cys
ENST00000410101.7:c.992T>G	ENSP00000386656.3:p.Phe331Cys
ENST00000467411.5:n.1769-779T>G
ENST00000496441.5:n.1878T>G
NM_031942.4:c.1124T>G	NP_114148.3:p.Phe375Cys
NM_145810.2:c.887T>G	NP_665809.1:p.Phe296Cys
XM_011511957.1:c.1043T>G	XP_011510259.1:p.Phe348Cys
XR_923034.1:n.2022T>G
NM_031942.5:c.1124T>G MANE Select	NP_114148.3:p.Phe375Cys
NM_145810.3:c.887T>G	NP_665809.1:p.Phe296Cys