Canonical Allele Identifier: CA349330665

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231077T>C (hg19) ; chr2:g.173366349T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366349T>C , CM000664.2:g.173366349T>C	GRCh38
NC_000002.11:g.174231077T>C , CM000664.1:g.174231077T>C	GRCh37
NC_000002.10:g.173939323T>C	NCBI36
NG_047202.1:g.17333T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+757T>C	ENSP00000512251.1:n.798+757T>C
ENST00000695911.1:c.880T>C	ENSP00000512262.1:n.880T>C
ENST00000695912.1:c.1099T>C	ENSP00000512263.1:p.Cys367Arg
ENST00000695913.1:c.*1855T>C	ENSP00000512264.1:n.*1855T>C
ENST00000695914.1:c.862T>C	ENSP00000512265.1:p.Cys288Arg
ENST00000695918.1:n.330T>C
ENST00000306721.8:c.1102T>C MANE Select	ENSP00000306968.3:p.Cys368Arg
ENST00000306721.7:c.1102T>C	ENSP00000306968.3:p.Cys368Arg
ENST00000347703.7:c.865T>C	ENSP00000272789.4:p.Cys289Arg
ENST00000410019.3:c.739T>C	ENSP00000386833.3:p.Cys247Arg
ENST00000410101.7:c.970T>C	ENSP00000386656.3:p.Cys324Arg
ENST00000467411.5:n.1768+757T>C
ENST00000496441.5:n.1856T>C
NM_031942.4:c.1102T>C	NP_114148.3:p.Cys368Arg
NM_145810.2:c.865T>C	NP_665809.1:p.Cys289Arg
XM_011511957.1:c.1021T>C	XP_011510259.1:p.Cys341Arg
XR_923034.1:n.2000T>C
NM_031942.5:c.1102T>C MANE Select	NP_114148.3:p.Cys368Arg
NM_145810.3:c.865T>C	NP_665809.1:p.Cys289Arg