Canonical Allele Identifier: CA349331083

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231155G>A (hg19) ; chr2:g.173366427G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366427G>A , CM000664.2:g.173366427G>A	GRCh38
NC_000002.11:g.174231155G>A , CM000664.1:g.174231155G>A	GRCh37
NC_000002.10:g.173939401G>A	NCBI36
NG_047202.1:g.17411G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-723G>A	ENSP00000512251.1:n.799-723G>A
ENST00000695911.1:c.958G>A	ENSP00000512262.1:n.958G>A
ENST00000695912.1:c.1177G>A	ENSP00000512263.1:p.Asp393Asn
ENST00000695913.1:c.*1933G>A	ENSP00000512264.1:n.*1933G>A
ENST00000695914.1:c.940G>A	ENSP00000512265.1:p.Asp314Asn
ENST00000695918.1:n.408G>A
ENST00000306721.8:c.1180G>A MANE Select	ENSP00000306968.3:p.Asp394Asn
ENST00000306721.7:c.1180G>A	ENSP00000306968.3:p.Asp394Asn
ENST00000347703.7:c.943G>A	ENSP00000272789.4:p.Asp315Asn
ENST00000410019.3:c.817G>A	ENSP00000386833.3:p.Asp273Asn
ENST00000410101.7:c.1048G>A	ENSP00000386656.3:p.Asp350Asn
ENST00000467411.5:n.1769-723G>A
ENST00000496441.5:n.1934G>A
NM_031942.4:c.1180G>A	NP_114148.3:p.Asp394Asn
NM_145810.2:c.943G>A	NP_665809.1:p.Asp315Asn
XM_011511957.1:c.1099G>A	XP_011510259.1:p.Asp367Asn
XR_923034.1:n.2078G>A
NM_031942.5:c.1180G>A MANE Select	NP_114148.3:p.Asp394Asn
NM_145810.3:c.943G>A	NP_665809.1:p.Asp315Asn