Canonical Allele Identifier: CA349330492

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231048A>C (hg19) ; chr2:g.173366320A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366320A>C , CM000664.2:g.173366320A>C	GRCh38
NC_000002.11:g.174231048A>C , CM000664.1:g.174231048A>C	GRCh37
NC_000002.10:g.173939294A>C	NCBI36
NG_047202.1:g.17304A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+728A>C	ENSP00000512251.1:n.798+728A>C
ENST00000695911.1:c.851A>C	ENSP00000512262.1:n.851A>C
ENST00000695912.1:c.1070A>C	ENSP00000512263.1:p.Asp357Ala
ENST00000695913.1:c.*1826A>C	ENSP00000512264.1:n.*1826A>C
ENST00000695914.1:c.833A>C	ENSP00000512265.1:p.Asp278Ala
ENST00000695918.1:n.301A>C
ENST00000306721.8:c.1073A>C MANE Select	ENSP00000306968.3:p.Asp358Ala
ENST00000306721.7:c.1073A>C	ENSP00000306968.3:p.Asp358Ala
ENST00000347703.7:c.836A>C	ENSP00000272789.4:p.Asp279Ala
ENST00000410019.3:c.710A>C	ENSP00000386833.3:p.Asp237Ala
ENST00000410101.7:c.941A>C	ENSP00000386656.3:p.Asp314Ala
ENST00000467411.5:n.1768+728A>C
ENST00000496441.5:n.1827A>C
NM_031942.4:c.1073A>C	NP_114148.3:p.Asp358Ala
NM_145810.2:c.836A>C	NP_665809.1:p.Asp279Ala
XM_011511957.1:c.992A>C	XP_011510259.1:p.Asp331Ala
XR_923034.1:n.1971A>C
NM_031942.5:c.1073A>C MANE Select	NP_114148.3:p.Asp358Ala
NM_145810.3:c.836A>C	NP_665809.1:p.Asp279Ala