Canonical Allele Identifier: CA349330843

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231112C>G (hg19) ; chr2:g.173366384C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366384C>G , CM000664.2:g.173366384C>G	GRCh38
NC_000002.11:g.174231112C>G , CM000664.1:g.174231112C>G	GRCh37
NC_000002.10:g.173939358C>G	NCBI36
NG_047202.1:g.17368C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-766C>G	ENSP00000512251.1:n.799-766C>G
ENST00000695911.1:c.915C>G	ENSP00000512262.1:n.915C>G
ENST00000695912.1:c.1134C>G	ENSP00000512263.1:p.Cys378Trp
ENST00000695913.1:c.*1890C>G	ENSP00000512264.1:n.*1890C>G
ENST00000695914.1:c.897C>G	ENSP00000512265.1:p.Cys299Trp
ENST00000695918.1:n.365C>G
ENST00000306721.8:c.1137C>G MANE Select	ENSP00000306968.3:p.Cys379Trp
ENST00000306721.7:c.1137C>G	ENSP00000306968.3:p.Cys379Trp
ENST00000347703.7:c.900C>G	ENSP00000272789.4:p.Cys300Trp
ENST00000410019.3:c.774C>G	ENSP00000386833.3:p.Cys258Trp
ENST00000410101.7:c.1005C>G	ENSP00000386656.3:p.Cys335Trp
ENST00000467411.5:n.1769-766C>G
ENST00000496441.5:n.1891C>G
NM_031942.4:c.1137C>G	NP_114148.3:p.Cys379Trp
NM_145810.2:c.900C>G	NP_665809.1:p.Cys300Trp
XM_011511957.1:c.1056C>G	XP_011510259.1:p.Cys352Trp
XR_923034.1:n.2035C>G
NM_031942.5:c.1137C>G MANE Select	NP_114148.3:p.Cys379Trp
NM_145810.3:c.900C>G	NP_665809.1:p.Cys300Trp