Canonical Allele Identifier: CA2661982989

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366255-G-GTTTTTTTTTTTTTTTTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366263_173366264insTTTTTTTTGTTTTTTTTT , CM000664.2:g.173366263_173366264insTTTTTTTTGTTTTTTTTT	GRCh38
NC_000002.11:g.174230991_174230992insTTTTTTTTGTTTTTTTTT , CM000664.1:g.174230991_174230992insTTTTTTTTGTTTTTTTTT	GRCh37
NC_000002.10:g.173939237_173939238insTTTTTTTTGTTTTTTTTT	NCBI36
NG_047202.1:g.17247_17248insTTTTTTTTGTTTTTTTTT

Transcript Alleles

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