Canonical Allele Identifier: CA349331036

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231147C>A (hg19) ; chr2:g.173366419C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366419C>A , CM000664.2:g.173366419C>A	GRCh38
NC_000002.11:g.174231147C>A , CM000664.1:g.174231147C>A	GRCh37
NC_000002.10:g.173939393C>A	NCBI36
NG_047202.1:g.17403C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-731C>A	ENSP00000512251.1:n.799-731C>A
ENST00000695911.1:c.950C>A	ENSP00000512262.1:n.950C>A
ENST00000695912.1:c.1169C>A	ENSP00000512263.1:p.Ala390Asp
ENST00000695913.1:c.*1925C>A	ENSP00000512264.1:n.*1925C>A
ENST00000695914.1:c.932C>A	ENSP00000512265.1:p.Ala311Asp
ENST00000695918.1:n.400C>A
ENST00000306721.8:c.1172C>A MANE Select	ENSP00000306968.3:p.Ala391Asp
ENST00000306721.7:c.1172C>A	ENSP00000306968.3:p.Ala391Asp
ENST00000347703.7:c.935C>A	ENSP00000272789.4:p.Ala312Asp
ENST00000410019.3:c.809C>A	ENSP00000386833.3:p.Ala270Asp
ENST00000410101.7:c.1040C>A	ENSP00000386656.3:p.Ala347Asp
ENST00000467411.5:n.1769-731C>A
ENST00000496441.5:n.1926C>A
NM_031942.4:c.1172C>A	NP_114148.3:p.Ala391Asp
NM_145810.2:c.935C>A	NP_665809.1:p.Ala312Asp
XM_011511957.1:c.1091C>A	XP_011510259.1:p.Ala364Asp
XR_923034.1:n.2070C>A
NM_031942.5:c.1172C>A MANE Select	NP_114148.3:p.Ala391Asp
NM_145810.3:c.935C>A	NP_665809.1:p.Ala312Asp