Canonical Allele Identifier: CA349331104

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231159C>G (hg19) ; chr2:g.173366431C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366431C>G , CM000664.2:g.173366431C>G	GRCh38
NC_000002.11:g.174231159C>G , CM000664.1:g.174231159C>G	GRCh37
NC_000002.10:g.173939405C>G	NCBI36
NG_047202.1:g.17415C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-719C>G	ENSP00000512251.1:n.799-719C>G
ENST00000695911.1:c.962C>G	ENSP00000512262.1:n.962C>G
ENST00000695912.1:c.1181C>G	ENSP00000512263.1:p.Pro394Arg
ENST00000695913.1:c.*1937C>G	ENSP00000512264.1:n.*1937C>G
ENST00000695914.1:c.944C>G	ENSP00000512265.1:p.Pro315Arg
ENST00000695918.1:n.412C>G
ENST00000306721.8:c.1184C>G MANE Select	ENSP00000306968.3:p.Pro395Arg
ENST00000306721.7:c.1184C>G	ENSP00000306968.3:p.Pro395Arg
ENST00000347703.7:c.947C>G	ENSP00000272789.4:p.Pro316Arg
ENST00000410019.3:c.821C>G	ENSP00000386833.3:p.Pro274Arg
ENST00000410101.7:c.1052C>G	ENSP00000386656.3:p.Pro351Arg
ENST00000467411.5:n.1769-719C>G
ENST00000496441.5:n.1938C>G
NM_031942.4:c.1184C>G	NP_114148.3:p.Pro395Arg
NM_145810.2:c.947C>G	NP_665809.1:p.Pro316Arg
XM_011511957.1:c.1103C>G	XP_011510259.1:p.Pro368Arg
XR_923034.1:n.2082C>G
NM_031942.5:c.1184C>G MANE Select	NP_114148.3:p.Pro395Arg
NM_145810.3:c.947C>G	NP_665809.1:p.Pro316Arg