Canonical Allele Identifier: CA1971419

Gene: CDCA7

Linked Data

• dbSNP Id: rs575009166
• ExAC: 2:174230975 T / G
• gnomAD v2: 2-174230975-T-G
• gnomAD v3: 2-173366247-T-G
• gnomAD v4: 2-173366247-T-G
• MyVariant Identifiers: chr2:g.174230975T>G (hg19) ; chr2:g.174230975_174230983delinsGTTTTTTTG (hg19) ; chr2:g.173366247T>G (hg38) ; chr2:g.173366247_173366255delinsGTTTTTTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366247T>G , CM000664.2:g.173366247T>G	GRCh38
NC_000002.11:g.174230975T>G , CM000664.1:g.174230975T>G	GRCh37
NC_000002.10:g.173939221T>G	NCBI36
NG_047202.1:g.17231T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+655T>G	ENSP00000512251.1:n.798+655T>G
ENST00000695911.1:c.814-36T>G	ENSP00000512262.1:n.814-36T>G
ENST00000695912.1:c.1033-36T>G	ENSP00000512263.1:n.1033-36T>G
ENST00000695913.1:c.*1753T>G	ENSP00000512264.1:n.*1753T>G
ENST00000695914.1:c.796-36T>G	ENSP00000512265.1:n.796-36T>G
ENST00000695918.1:n.264-36T>G
ENST00000306721.8:c.1036-36T>G MANE Select	ENSP00000306968.3:n.1036-36T>G
ENST00000306721.7:c.1036-36T>G	ENSP00000306968.3:n.1036-36T>G
ENST00000347703.7:c.799-36T>G	ENSP00000272789.4:n.799-36T>G
ENST00000410019.3:c.673-36T>G	ENSP00000386833.3:n.673-36T>G
ENST00000410101.7:c.904-36T>G	ENSP00000386656.3:n.904-36T>G
ENST00000467411.5:n.1768+655T>G
ENST00000496441.5:n.1790-36T>G
NM_031942.4:c.1036-36T>G	NP_114148.3:n.1036-36T>G
NM_145810.2:c.799-36T>G	NP_665809.1:n.799-36T>G
XM_011511957.1:c.955-36T>G	XP_011510259.1:n.955-36T>G
XR_923034.1:n.1934-36T>G
NM_031942.5:c.1036-36T>G MANE Select	NP_114148.3:n.1036-36T>G
NM_145810.3:c.799-36T>G	NP_665809.1:n.799-36T>G