Canonical Allele Identifier: CA2661982983
Gene: CDCA7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.173366263_173366264insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.2:g.173366263_173366264insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000002.11:g.174230991_174230992insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.1:g.174230991_174230992insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000002.10:g.173939237_173939238insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_047202.1:g.17247_17248insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695901.1:c.798+671_798+672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000512251.1:n.798+671_798+672insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000695911.1:c.814-20_814-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000512262.1:n.814-20_814-19insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000695912.1:c.1033-20_1033-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000512263.1:n.1033-20_1033-19insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000695913.1:c.*1769_*1770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000512264.1:n.*1769_*1770insTTTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000695914.1:c.796-20_796-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000512265.1:n.796-20_796-19insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000695918.1:n.264-20_264-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000306721.8:c.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000306968.3:n.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000306721.7:c.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000306968.3:n.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000347703.7:c.799-20_799-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000272789.4:n.799-20_799-19insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000410019.3:c.673-20_673-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000386833.3:n.673-20_673-19insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000410101.7:c.904-20_904-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000386656.3:n.904-20_904-19insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000467411.5:n.1768+671_1768+672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000496441.5:n.1790-20_1790-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_031942.4:c.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_114148.3:n.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_145810.2:c.799-20_799-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_665809.1:n.799-20_799-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011511957.1:c.955-20_955-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011510259.1:n.955-20_955-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XR_923034.1:n.1934-20_1934-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_031942.5:c.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_114148.3:n.1036-20_1036-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_145810.3:c.799-20_799-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_665809.1:n.799-20_799-19insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...