Canonical Allele Identifier: CA429810492

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231088T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366360T>C , CM000664.2:g.173366360T>C	GRCh38
NC_000002.11:g.174231088T>C , CM000664.1:g.174231088T>C	GRCh37
NC_000002.10:g.173939334T>C	NCBI36
NG_047202.1:g.17344T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+768T>C	ENSP00000512251.1:n.798+768T>C
ENST00000695911.1:c.891T>C	ENSP00000512262.1:n.891T>C
ENST00000695912.1:c.1110T>C	ENSP00000512263.1:p.Val370=
ENST00000695913.1:c.*1866T>C	ENSP00000512264.1:n.*1866T>C
ENST00000695914.1:c.873T>C	ENSP00000512265.1:p.Val291=
ENST00000695918.1:n.341T>C
ENST00000306721.8:c.1113T>C MANE Select	ENSP00000306968.3:p.Val371=
ENST00000306721.7:c.1113T>C	ENSP00000306968.3:p.Val371=
ENST00000347703.7:c.876T>C	ENSP00000272789.4:p.Val292=
ENST00000410019.3:c.750T>C	ENSP00000386833.3:p.Val250=
ENST00000410101.7:c.981T>C	ENSP00000386656.3:p.Val327=
ENST00000467411.5:n.1768+768T>C
ENST00000496441.5:n.1867T>C
NM_031942.4:c.1113T>C	NP_114148.3:p.Val371=
NM_145810.2:c.876T>C	NP_665809.1:p.Val292=
XM_011511957.1:c.1032T>C	XP_011510259.1:p.Val344=
XR_923034.1:n.2011T>C
NM_031942.5:c.1113T>C MANE Select	NP_114148.3:p.Val371=
NM_145810.3:c.876T>C	NP_665809.1:p.Val292=