Canonical Allele Identifier: CA1971430

Gene: CDCA7

Linked Data

• dbSNP Id: rs768105204
• ExAC: 2:174230989 T / TA
• gnomAD v2: 2-174230989-T-TA
• gnomAD v3: 2-173366261-T-TA
• gnomAD v4: 2-173366261-T-TA
• MyVariant Identifiers: chr2:g.174230989_174230990insA (hg19) ; chr2:g.173366261_173366262insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366261_173366262insA , CM000664.2:g.173366261_173366262insA	GRCh38
NC_000002.11:g.174230989_174230990insA , CM000664.1:g.174230989_174230990insA	GRCh37
NC_000002.10:g.173939235_173939236insA	NCBI36
NG_047202.1:g.17245_17246insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+669_798+670insA	ENSP00000512251.1:n.798+669_798+670insA
ENST00000695911.1:c.814-22_814-21insA	ENSP00000512262.1:n.814-22_814-21insA
ENST00000695912.1:c.1033-22_1033-21insA	ENSP00000512263.1:n.1033-22_1033-21insA
ENST00000695913.1:c.*1767_*1768insA	ENSP00000512264.1:n.*1767_*1768insA
ENST00000695914.1:c.796-22_796-21insA	ENSP00000512265.1:n.796-22_796-21insA
ENST00000695918.1:n.264-22_264-21insA
ENST00000306721.8:c.1036-22_1036-21insA MANE Select	ENSP00000306968.3:n.1036-22_1036-21insA
ENST00000306721.7:c.1036-22_1036-21insA	ENSP00000306968.3:n.1036-22_1036-21insA
ENST00000347703.7:c.799-22_799-21insA	ENSP00000272789.4:n.799-22_799-21insA
ENST00000410019.3:c.673-22_673-21insA	ENSP00000386833.3:n.673-22_673-21insA
ENST00000410101.7:c.904-22_904-21insA	ENSP00000386656.3:n.904-22_904-21insA
ENST00000467411.5:n.1768+669_1768+670insA
ENST00000496441.5:n.1790-22_1790-21insA
NM_031942.4:c.1036-22_1036-21insA	NP_114148.3:n.1036-22_1036-21insA
NM_145810.2:c.799-22_799-21insA	NP_665809.1:n.799-22_799-21insA
XM_011511957.1:c.955-22_955-21insA	XP_011510259.1:n.955-22_955-21insA
XR_923034.1:n.1934-22_1934-21insA
NM_031942.5:c.1036-22_1036-21insA MANE Select	NP_114148.3:n.1036-22_1036-21insA
NM_145810.3:c.799-22_799-21insA	NP_665809.1:n.799-22_799-21insA