Canonical Allele Identifier: CA349330729

Gene: CDCA7

Linked Data

• dbSNP Id: rs1321106398
• gnomAD v3: 2-173366362-G-C
• gnomAD v4: 2-173366362-G-C
• MyVariant Identifiers: chr2:g.174231090G>C (hg19) ; chr2:g.173366362G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366362G>C , CM000664.2:g.173366362G>C	GRCh38
NC_000002.11:g.174231090G>C , CM000664.1:g.174231090G>C	GRCh37
NC_000002.10:g.173939336G>C	NCBI36
NG_047202.1:g.17346G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+770G>C	ENSP00000512251.1:n.798+770G>C
ENST00000695911.1:c.893G>C	ENSP00000512262.1:n.893G>C
ENST00000695912.1:c.1112G>C	ENSP00000512263.1:p.Arg371Pro
ENST00000695913.1:c.*1868G>C	ENSP00000512264.1:n.*1868G>C
ENST00000695914.1:c.875G>C	ENSP00000512265.1:p.Arg292Pro
ENST00000695918.1:n.343G>C
ENST00000306721.8:c.1115G>C MANE Select	ENSP00000306968.3:p.Arg372Pro
ENST00000306721.7:c.1115G>C	ENSP00000306968.3:p.Arg372Pro
ENST00000347703.7:c.878G>C	ENSP00000272789.4:p.Arg293Pro
ENST00000410019.3:c.752G>C	ENSP00000386833.3:p.Arg251Pro
ENST00000410101.7:c.983G>C	ENSP00000386656.3:p.Arg328Pro
ENST00000467411.5:n.1768+770G>C
ENST00000496441.5:n.1869G>C
NM_031942.4:c.1115G>C	NP_114148.3:p.Arg372Pro
NM_145810.2:c.878G>C	NP_665809.1:p.Arg293Pro
XM_011511957.1:c.1034G>C	XP_011510259.1:p.Arg345Pro
XR_923034.1:n.2013G>C
NM_031942.5:c.1115G>C MANE Select	NP_114148.3:p.Arg372Pro
NM_145810.3:c.878G>C	NP_665809.1:p.Arg293Pro