Canonical Allele Identifier: CA349330775

Gene: CDCA7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-779T>A	ENSP00000512251.1:n.799-779T>A
ENST00000695911.1:c.902T>A	ENSP00000512262.1:n.902T>A
ENST00000695912.1:c.1121T>A	ENSP00000512263.1:p.Phe374Tyr
ENST00000695913.1:c.*1877T>A	ENSP00000512264.1:n.*1877T>A
ENST00000695914.1:c.884T>A	ENSP00000512265.1:p.Phe295Tyr
ENST00000695918.1:n.352T>A
ENST00000306721.8:c.1124T>A MANE Select	ENSP00000306968.3:p.Phe375Tyr
ENST00000306721.7:c.1124T>A	ENSP00000306968.3:p.Phe375Tyr
ENST00000347703.7:c.887T>A	ENSP00000272789.4:p.Phe296Tyr
ENST00000410019.3:c.761T>A	ENSP00000386833.3:p.Phe254Tyr
ENST00000410101.7:c.992T>A	ENSP00000386656.3:p.Phe331Tyr
ENST00000467411.5:n.1769-779T>A
ENST00000496441.5:n.1878T>A
NM_031942.4:c.1124T>A	NP_114148.3:p.Phe375Tyr
NM_145810.2:c.887T>A	NP_665809.1:p.Phe296Tyr
XM_011511957.1:c.1043T>A	XP_011510259.1:p.Phe348Tyr
XR_923034.1:n.2022T>A
NM_031942.5:c.1124T>A MANE Select	NP_114148.3:p.Phe375Tyr
NM_145810.3:c.887T>A	NP_665809.1:p.Phe296Tyr