Canonical Allele Identifier: CA349330464

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231041A>C (hg19) ; chr2:g.173366313A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366313A>C , CM000664.2:g.173366313A>C	GRCh38
NC_000002.11:g.174231041A>C , CM000664.1:g.174231041A>C	GRCh37
NC_000002.10:g.173939287A>C	NCBI36
NG_047202.1:g.17297A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+721A>C	ENSP00000512251.1:n.798+721A>C
ENST00000695911.1:c.844A>C	ENSP00000512262.1:n.844A>C
ENST00000695912.1:c.1063A>C	ENSP00000512263.1:p.Thr355Pro
ENST00000695913.1:c.*1819A>C	ENSP00000512264.1:n.*1819A>C
ENST00000695914.1:c.826A>C	ENSP00000512265.1:p.Thr276Pro
ENST00000695918.1:n.294A>C
ENST00000306721.8:c.1066A>C MANE Select	ENSP00000306968.3:p.Thr356Pro
ENST00000306721.7:c.1066A>C	ENSP00000306968.3:p.Thr356Pro
ENST00000347703.7:c.829A>C	ENSP00000272789.4:p.Thr277Pro
ENST00000410019.3:c.703A>C	ENSP00000386833.3:p.Thr235Pro
ENST00000410101.7:c.934A>C	ENSP00000386656.3:p.Thr312Pro
ENST00000467411.5:n.1768+721A>C
ENST00000496441.5:n.1820A>C
NM_031942.4:c.1066A>C	NP_114148.3:p.Thr356Pro
NM_145810.2:c.829A>C	NP_665809.1:p.Thr277Pro
XM_011511957.1:c.985A>C	XP_011510259.1:p.Thr329Pro
XR_923034.1:n.1964A>C
NM_031942.5:c.1066A>C MANE Select	NP_114148.3:p.Thr356Pro
NM_145810.3:c.829A>C	NP_665809.1:p.Thr277Pro