Canonical Allele Identifier: CA349330807

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231104G>C (hg19) ; chr2:g.173366376G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366376G>C , CM000664.2:g.173366376G>C	GRCh38
NC_000002.11:g.174231104G>C , CM000664.1:g.174231104G>C	GRCh37
NC_000002.10:g.173939350G>C	NCBI36
NG_047202.1:g.17360G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-774G>C	ENSP00000512251.1:n.799-774G>C
ENST00000695911.1:c.907G>C	ENSP00000512262.1:n.907G>C
ENST00000695912.1:c.1126G>C	ENSP00000512263.1:p.Gly376Arg
ENST00000695913.1:c.*1882G>C	ENSP00000512264.1:n.*1882G>C
ENST00000695914.1:c.889G>C	ENSP00000512265.1:p.Gly297Arg
ENST00000695918.1:n.357G>C
ENST00000306721.8:c.1129G>C MANE Select	ENSP00000306968.3:p.Gly377Arg
ENST00000306721.7:c.1129G>C	ENSP00000306968.3:p.Gly377Arg
ENST00000347703.7:c.892G>C	ENSP00000272789.4:p.Gly298Arg
ENST00000410019.3:c.766G>C	ENSP00000386833.3:p.Gly256Arg
ENST00000410101.7:c.997G>C	ENSP00000386656.3:p.Gly333Arg
ENST00000467411.5:n.1769-774G>C
ENST00000496441.5:n.1883G>C
NM_031942.4:c.1129G>C	NP_114148.3:p.Gly377Arg
NM_145810.2:c.892G>C	NP_665809.1:p.Gly298Arg
XM_011511957.1:c.1048G>C	XP_011510259.1:p.Gly350Arg
XR_923034.1:n.2027G>C
NM_031942.5:c.1129G>C MANE Select	NP_114148.3:p.Gly377Arg
NM_145810.3:c.892G>C	NP_665809.1:p.Gly298Arg