Canonical Allele Identifier: CA349330478

Gene: CDCA7

Linked Data

• dbSNP Id: rs1428520878
• gnomAD v4: 2-173366317-T-C
• MyVariant Identifiers: chr2:g.174231045T>C (hg19) ; chr2:g.173366317T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366317T>C , CM000664.2:g.173366317T>C	GRCh38
NC_000002.11:g.174231045T>C , CM000664.1:g.174231045T>C	GRCh37
NC_000002.10:g.173939291T>C	NCBI36
NG_047202.1:g.17301T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+725T>C	ENSP00000512251.1:n.798+725T>C
ENST00000695911.1:c.848T>C	ENSP00000512262.1:n.848T>C
ENST00000695912.1:c.1067T>C	ENSP00000512263.1:p.Ile356Thr
ENST00000695913.1:c.*1823T>C	ENSP00000512264.1:n.*1823T>C
ENST00000695914.1:c.830T>C	ENSP00000512265.1:p.Ile277Thr
ENST00000695918.1:n.298T>C
ENST00000306721.8:c.1070T>C MANE Select	ENSP00000306968.3:p.Ile357Thr
ENST00000306721.7:c.1070T>C	ENSP00000306968.3:p.Ile357Thr
ENST00000347703.7:c.833T>C	ENSP00000272789.4:p.Ile278Thr
ENST00000410019.3:c.707T>C	ENSP00000386833.3:p.Ile236Thr
ENST00000410101.7:c.938T>C	ENSP00000386656.3:p.Ile313Thr
ENST00000467411.5:n.1768+725T>C
ENST00000496441.5:n.1824T>C
NM_031942.4:c.1070T>C	NP_114148.3:p.Ile357Thr
NM_145810.2:c.833T>C	NP_665809.1:p.Ile278Thr
XM_011511957.1:c.989T>C	XP_011510259.1:p.Ile330Thr
XR_923034.1:n.1968T>C
NM_031942.5:c.1070T>C MANE Select	NP_114148.3:p.Ile357Thr
NM_145810.3:c.833T>C	NP_665809.1:p.Ile278Thr