Canonical Allele Identifier: CA60779985

Gene: CDCA7

Linked Data

• dbSNP Id: rs397809331
• gnomAD v2: 2-174230991-T-TC
• gnomAD v3: 2-173366263-T-TC
• gnomAD v4: 2-173366263-T-TC
• MyVariant Identifiers: chr2:g.174230991_174230992insC (hg19) ; chr2:g.173366263_173366264insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366264dup , CM000664.2:g.173366264dup	GRCh38
NC_000002.11:g.174230992dup , CM000664.1:g.174230992dup	GRCh37
NC_000002.10:g.173939238dup	NCBI36
NG_047202.1:g.17248dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+672dup	ENSP00000512251.1:n.798+672dup
ENST00000695911.1:c.814-19dup	ENSP00000512262.1:n.814-19dup
ENST00000695912.1:c.1033-19dup	ENSP00000512263.1:n.1033-19dup
ENST00000695913.1:c.*1770dup	ENSP00000512264.1:n.*1770dup
ENST00000695914.1:c.796-19dup	ENSP00000512265.1:n.796-19dup
ENST00000695918.1:n.264-19dup
ENST00000306721.8:c.1036-19dup MANE Select	ENSP00000306968.3:n.1036-19dup
ENST00000306721.7:c.1036-19dup	ENSP00000306968.3:n.1036-19dup
ENST00000347703.7:c.799-19dup	ENSP00000272789.4:n.799-19dup
ENST00000410019.3:c.673-19dup	ENSP00000386833.3:n.673-19dup
ENST00000410101.7:c.904-19dup	ENSP00000386656.3:n.904-19dup
ENST00000467411.5:n.1768+672dup
ENST00000496441.5:n.1790-19dup
NM_031942.4:c.1036-19dup	NP_114148.3:n.1036-19dup
NM_145810.2:c.799-19dup	NP_665809.1:n.799-19dup
XM_011511957.1:c.955-19dup	XP_011510259.1:n.955-19dup
XR_923034.1:n.1934-19dup
NM_031942.5:c.1036-19dup MANE Select	NP_114148.3:n.1036-19dup
NM_145810.3:c.799-19dup	NP_665809.1:n.799-19dup