Canonical Allele Identifier: CA1308216425

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366346G= , CM000664.2:g.173366346G=	GRCh38
NC_000002.11:g.174231074G= , CM000664.1:g.174231074G=	GRCh37
NC_000002.10:g.173939320G=	NCBI36
NG_047202.1:g.17330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+754G=	ENSP00000512251.1:n.798+754G=
ENST00000695911.1:c.877G=	ENSP00000512262.1:n.877G=
ENST00000695912.1:c.1096G=	ENSP00000512263.1:p.Asp366=
ENST00000695913.1:c.*1852G=	ENSP00000512264.1:n.*1852G=
ENST00000695914.1:c.859G=	ENSP00000512265.1:p.Asp287=
ENST00000695918.1:n.327G=
ENST00000306721.8:c.1099G= MANE Select	ENSP00000306968.3:p.Asp367=
ENST00000306721.7:c.1099G=	ENSP00000306968.3:p.Asp367=
ENST00000347703.7:c.862G=	ENSP00000272789.4:p.Asp288=
ENST00000410019.3:c.736G=	ENSP00000386833.3:p.Asp246=
ENST00000410101.7:c.967G=	ENSP00000386656.3:p.Asp323=
ENST00000467411.5:n.1768+754G=
ENST00000496441.5:n.1853G=
NM_031942.4:c.1099G=	NP_114148.3:p.Asp367=
NM_145810.2:c.862G=	NP_665809.1:p.Asp288=
XM_011511957.1:c.1018G=	XP_011510259.1:p.Asp340=
XR_923034.1:n.1997G=
NM_031942.5:c.1099G= MANE Select	NP_114148.3:p.Asp367=
NM_145810.3:c.862G=	NP_665809.1:p.Asp288=