Canonical Allele Identifier: CA1308216324

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366121G= , CM000664.2:g.173366121G=	GRCh38
NC_000002.11:g.174230849G= , CM000664.1:g.174230849G=	GRCh37
NC_000002.10:g.173939095G=	NCBI36
NG_047202.1:g.17105G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+529G=	ENSP00000512251.1:n.798+529G=
ENST00000695911.1:c.814-162G=	ENSP00000512262.1:n.814-162G=
ENST00000695912.1:c.1033-162G=	ENSP00000512263.1:n.1033-162G=
ENST00000695913.1:c.*1627G=	ENSP00000512264.1:n.*1627G=
ENST00000695914.1:c.796-162G=	ENSP00000512265.1:n.796-162G=
ENST00000695918.1:n.264-162G=
ENST00000306721.8:c.1036-162G= MANE Select	ENSP00000306968.3:n.1036-162G=
ENST00000306721.7:c.1036-162G=	ENSP00000306968.3:n.1036-162G=
ENST00000347703.7:c.799-162G=	ENSP00000272789.4:n.799-162G=
ENST00000410019.3:c.673-162G=	ENSP00000386833.3:n.673-162G=
ENST00000410101.7:c.904-162G=	ENSP00000386656.3:n.904-162G=
ENST00000467411.5:n.1768+529G=
ENST00000496441.5:n.1790-162G=
NM_031942.4:c.1036-162G=	NP_114148.3:n.1036-162G=
NM_145810.2:c.799-162G=	NP_665809.1:n.799-162G=
XM_011511957.1:c.955-162G=	XP_011510259.1:n.955-162G=
XR_923034.1:n.1934-162G=
NM_031942.5:c.1036-162G= MANE Select	NP_114148.3:n.1036-162G=
NM_145810.3:c.799-162G=	NP_665809.1:n.799-162G=