Canonical Allele Identifier: CA1308216441

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366386T= , CM000664.2:g.173366386T=	GRCh38
NC_000002.11:g.174231114T= , CM000664.1:g.174231114T=	GRCh37
NC_000002.10:g.173939360T=	NCBI36
NG_047202.1:g.17370T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-764T=	ENSP00000512251.1:n.799-764T=
ENST00000695911.1:c.917T=	ENSP00000512262.1:n.917T=
ENST00000695912.1:c.1136T=	ENSP00000512263.1:p.Leu379=
ENST00000695913.1:c.*1892T=	ENSP00000512264.1:n.*1892T=
ENST00000695914.1:c.899T=	ENSP00000512265.1:p.Leu300=
ENST00000695918.1:n.367T=
ENST00000306721.8:c.1139T= MANE Select	ENSP00000306968.3:p.Leu380=
ENST00000306721.7:c.1139T=	ENSP00000306968.3:p.Leu380=
ENST00000347703.7:c.902T=	ENSP00000272789.4:p.Leu301=
ENST00000410019.3:c.776T=	ENSP00000386833.3:p.Leu259=
ENST00000410101.7:c.1007T=	ENSP00000386656.3:p.Leu336=
ENST00000467411.5:n.1769-764T=
ENST00000496441.5:n.1893T=
NM_031942.4:c.1139T=	NP_114148.3:p.Leu380=
NM_145810.2:c.902T=	NP_665809.1:p.Leu301=
XM_011511957.1:c.1058T=	XP_011510259.1:p.Leu353=
XR_923034.1:n.2037T=
NM_031942.5:c.1139T= MANE Select	NP_114148.3:p.Leu380=
NM_145810.3:c.902T=	NP_665809.1:p.Leu301=