Canonical Allele Identifier: CA1308216454

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366432G= , CM000664.2:g.173366432G=	GRCh38
NC_000002.11:g.174231160G= , CM000664.1:g.174231160G=	GRCh37
NC_000002.10:g.173939406G=	NCBI36
NG_047202.1:g.17416G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-718G=	ENSP00000512251.1:n.799-718G=
ENST00000695911.1:c.963G=	ENSP00000512262.1:n.963G=
ENST00000695912.1:c.1182G=	ENSP00000512263.1:p.Pro394=
ENST00000695913.1:c.*1938G=	ENSP00000512264.1:n.*1938G=
ENST00000695914.1:c.945G=	ENSP00000512265.1:p.Pro315=
ENST00000695918.1:n.413G=
ENST00000306721.8:c.1185G= MANE Select	ENSP00000306968.3:p.Pro395=
ENST00000306721.7:c.1185G=	ENSP00000306968.3:p.Pro395=
ENST00000347703.7:c.948G=	ENSP00000272789.4:p.Pro316=
ENST00000410019.3:c.822G=	ENSP00000386833.3:p.Pro274=
ENST00000410101.7:c.1053G=	ENSP00000386656.3:p.Pro351=
ENST00000467411.5:n.1769-718G=
ENST00000496441.5:n.1939G=
NM_031942.4:c.1185G=	NP_114148.3:p.Pro395=
NM_145810.2:c.948G=	NP_665809.1:p.Pro316=
XM_011511957.1:c.1104G=	XP_011510259.1:p.Pro368=
XR_923034.1:n.2083G=
NM_031942.5:c.1185G= MANE Select	NP_114148.3:p.Pro395=
NM_145810.3:c.948G=	NP_665809.1:p.Pro316=