Canonical Allele Identifier: CA349330546

Gene: CDCA7

Linked Data

• dbSNP Id: rs1384655129
• gnomAD v2: 2-174231057-C-G
• gnomAD v4: 2-173366329-C-G
• MyVariant Identifiers: chr2:g.174231057C>G (hg19) ; chr2:g.173366329C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366329C>G , CM000664.2:g.173366329C>G	GRCh38
NC_000002.11:g.174231057C>G , CM000664.1:g.174231057C>G	GRCh37
NC_000002.10:g.173939303C>G	NCBI36
NG_047202.1:g.17313C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+737C>G	ENSP00000512251.1:n.798+737C>G
ENST00000695911.1:c.860C>G	ENSP00000512262.1:n.860C>G
ENST00000695912.1:c.1079C>G	ENSP00000512263.1:p.Thr360Arg
ENST00000695913.1:c.*1835C>G	ENSP00000512264.1:n.*1835C>G
ENST00000695914.1:c.842C>G	ENSP00000512265.1:p.Thr281Arg
ENST00000695918.1:n.310C>G
ENST00000306721.8:c.1082C>G MANE Select	ENSP00000306968.3:p.Thr361Arg
ENST00000306721.7:c.1082C>G	ENSP00000306968.3:p.Thr361Arg
ENST00000347703.7:c.845C>G	ENSP00000272789.4:p.Thr282Arg
ENST00000410019.3:c.719C>G	ENSP00000386833.3:p.Thr240Arg
ENST00000410101.7:c.950C>G	ENSP00000386656.3:p.Thr317Arg
ENST00000467411.5:n.1768+737C>G
ENST00000496441.5:n.1836C>G
NM_031942.4:c.1082C>G	NP_114148.3:p.Thr361Arg
NM_145810.2:c.845C>G	NP_665809.1:p.Thr282Arg
XM_011511957.1:c.1001C>G	XP_011510259.1:p.Thr334Arg
XR_923034.1:n.1980C>G
NM_031942.5:c.1082C>G MANE Select	NP_114148.3:p.Thr361Arg
NM_145810.3:c.845C>G	NP_665809.1:p.Thr282Arg