Canonical Allele Identifier: CA1308216365
Gene: CDCA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.173366219T= , CM000664.2:g.173366219T= GRCh38
NC_000002.11:g.174230947T= , CM000664.1:g.174230947T= GRCh37
NC_000002.10:g.173939193T= NCBI36
NG_047202.1:g.17203T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695901.1:c.798+627T= ENSP00000512251.1:n.798+627T=
ENST00000695911.1:c.814-64T= ENSP00000512262.1:n.814-64T=
ENST00000695912.1:c.1033-64T= ENSP00000512263.1:n.1033-64T=
ENST00000695913.1:c.*1725T= ENSP00000512264.1:n.*1725T=
ENST00000695914.1:c.796-64T= ENSP00000512265.1:n.796-64T=
ENST00000695918.1:n.264-64T=
ENST00000306721.8:c.1036-64T= MANE Select ENSP00000306968.3:n.1036-64T=
ENST00000306721.7:c.1036-64T= ENSP00000306968.3:n.1036-64T=
ENST00000347703.7:c.799-64T= ENSP00000272789.4:n.799-64T=
ENST00000410019.3:c.673-64T= ENSP00000386833.3:n.673-64T=
ENST00000410101.7:c.904-64T= ENSP00000386656.3:n.904-64T=
ENST00000467411.5:n.1768+627T=
ENST00000496441.5:n.1790-64T=
NM_031942.4:c.1036-64T= NP_114148.3:n.1036-64T=
NM_145810.2:c.799-64T= NP_665809.1:n.799-64T=
XM_011511957.1:c.955-64T= XP_011510259.1:n.955-64T=
XR_923034.1:n.1934-64T=
NM_031942.5:c.1036-64T= MANE Select NP_114148.3:n.1036-64T=
NM_145810.3:c.799-64T= NP_665809.1:n.799-64T=