Canonical Allele Identifier: CA349330476

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231044A>T (hg19) ; chr2:g.173366316A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366316A>T , CM000664.2:g.173366316A>T	GRCh38
NC_000002.11:g.174231044A>T , CM000664.1:g.174231044A>T	GRCh37
NC_000002.10:g.173939290A>T	NCBI36
NG_047202.1:g.17300A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+724A>T	ENSP00000512251.1:n.798+724A>T
ENST00000695911.1:c.847A>T	ENSP00000512262.1:n.847A>T
ENST00000695912.1:c.1066A>T	ENSP00000512263.1:p.Ile356Phe
ENST00000695913.1:c.*1822A>T	ENSP00000512264.1:n.*1822A>T
ENST00000695914.1:c.829A>T	ENSP00000512265.1:p.Ile277Phe
ENST00000695918.1:n.297A>T
ENST00000306721.8:c.1069A>T MANE Select	ENSP00000306968.3:p.Ile357Phe
ENST00000306721.7:c.1069A>T	ENSP00000306968.3:p.Ile357Phe
ENST00000347703.7:c.832A>T	ENSP00000272789.4:p.Ile278Phe
ENST00000410019.3:c.706A>T	ENSP00000386833.3:p.Ile236Phe
ENST00000410101.7:c.937A>T	ENSP00000386656.3:p.Ile313Phe
ENST00000467411.5:n.1768+724A>T
ENST00000496441.5:n.1823A>T
NM_031942.4:c.1069A>T	NP_114148.3:p.Ile357Phe
NM_145810.2:c.832A>T	NP_665809.1:p.Ile278Phe
XM_011511957.1:c.988A>T	XP_011510259.1:p.Ile330Phe
XR_923034.1:n.1967A>T
NM_031942.5:c.1069A>T MANE Select	NP_114148.3:p.Ile357Phe
NM_145810.3:c.832A>T	NP_665809.1:p.Ile278Phe