Canonical Allele Identifier: CA349330586

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231064C>G (hg19) ; chr2:g.173366336C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366336C>G , CM000664.2:g.173366336C>G	GRCh38
NC_000002.11:g.174231064C>G , CM000664.1:g.174231064C>G	GRCh37
NC_000002.10:g.173939310C>G	NCBI36
NG_047202.1:g.17320C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+744C>G	ENSP00000512251.1:n.798+744C>G
ENST00000695911.1:c.867C>G	ENSP00000512262.1:n.867C>G
ENST00000695912.1:c.1086C>G	ENSP00000512263.1:p.Cys362Trp
ENST00000695913.1:c.*1842C>G	ENSP00000512264.1:n.*1842C>G
ENST00000695914.1:c.849C>G	ENSP00000512265.1:p.Cys283Trp
ENST00000695918.1:n.317C>G
ENST00000306721.8:c.1089C>G MANE Select	ENSP00000306968.3:p.Cys363Trp
ENST00000306721.7:c.1089C>G	ENSP00000306968.3:p.Cys363Trp
ENST00000347703.7:c.852C>G	ENSP00000272789.4:p.Cys284Trp
ENST00000410019.3:c.726C>G	ENSP00000386833.3:p.Cys242Trp
ENST00000410101.7:c.957C>G	ENSP00000386656.3:p.Cys319Trp
ENST00000467411.5:n.1768+744C>G
ENST00000496441.5:n.1843C>G
NM_031942.4:c.1089C>G	NP_114148.3:p.Cys363Trp
NM_145810.2:c.852C>G	NP_665809.1:p.Cys284Trp
XM_011511957.1:c.1008C>G	XP_011510259.1:p.Cys336Trp
XR_923034.1:n.1987C>G
NM_031942.5:c.1089C>G MANE Select	NP_114148.3:p.Cys363Trp
NM_145810.3:c.852C>G	NP_665809.1:p.Cys284Trp