Canonical Allele Identifier: CA349330819

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231107C>G (hg19) ; chr2:g.173366379C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366379C>G , CM000664.2:g.173366379C>G	GRCh38
NC_000002.11:g.174231107C>G , CM000664.1:g.174231107C>G	GRCh37
NC_000002.10:g.173939353C>G	NCBI36
NG_047202.1:g.17363C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-771C>G	ENSP00000512251.1:n.799-771C>G
ENST00000695911.1:c.910C>G	ENSP00000512262.1:n.910C>G
ENST00000695912.1:c.1129C>G	ENSP00000512263.1:p.Pro377Ala
ENST00000695913.1:c.*1885C>G	ENSP00000512264.1:n.*1885C>G
ENST00000695914.1:c.892C>G	ENSP00000512265.1:p.Pro298Ala
ENST00000695918.1:n.360C>G
ENST00000306721.8:c.1132C>G MANE Select	ENSP00000306968.3:p.Pro378Ala
ENST00000306721.7:c.1132C>G	ENSP00000306968.3:p.Pro378Ala
ENST00000347703.7:c.895C>G	ENSP00000272789.4:p.Pro299Ala
ENST00000410019.3:c.769C>G	ENSP00000386833.3:p.Pro257Ala
ENST00000410101.7:c.1000C>G	ENSP00000386656.3:p.Pro334Ala
ENST00000467411.5:n.1769-771C>G
ENST00000496441.5:n.1886C>G
NM_031942.4:c.1132C>G	NP_114148.3:p.Pro378Ala
NM_145810.2:c.895C>G	NP_665809.1:p.Pro299Ala
XM_011511957.1:c.1051C>G	XP_011510259.1:p.Pro351Ala
XR_923034.1:n.2030C>G
NM_031942.5:c.1132C>G MANE Select	NP_114148.3:p.Pro378Ala
NM_145810.3:c.895C>G	NP_665809.1:p.Pro299Ala