Canonical Allele Identifier: CA349330824

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366380-C-G
• MyVariant Identifiers: chr2:g.174231108C>G (hg19) ; chr2:g.173366380C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366380C>G , CM000664.2:g.173366380C>G	GRCh38
NC_000002.11:g.174231108C>G , CM000664.1:g.174231108C>G	GRCh37
NC_000002.10:g.173939354C>G	NCBI36
NG_047202.1:g.17364C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-770C>G	ENSP00000512251.1:n.799-770C>G
ENST00000695911.1:c.911C>G	ENSP00000512262.1:n.911C>G
ENST00000695912.1:c.1130C>G	ENSP00000512263.1:p.Pro377Arg
ENST00000695913.1:c.*1886C>G	ENSP00000512264.1:n.*1886C>G
ENST00000695914.1:c.893C>G	ENSP00000512265.1:p.Pro298Arg
ENST00000695918.1:n.361C>G
ENST00000306721.8:c.1133C>G MANE Select	ENSP00000306968.3:p.Pro378Arg
ENST00000306721.7:c.1133C>G	ENSP00000306968.3:p.Pro378Arg
ENST00000347703.7:c.896C>G	ENSP00000272789.4:p.Pro299Arg
ENST00000410019.3:c.770C>G	ENSP00000386833.3:p.Pro257Arg
ENST00000410101.7:c.1001C>G	ENSP00000386656.3:p.Pro334Arg
ENST00000467411.5:n.1769-770C>G
ENST00000496441.5:n.1887C>G
NM_031942.4:c.1133C>G	NP_114148.3:p.Pro378Arg
NM_145810.2:c.896C>G	NP_665809.1:p.Pro299Arg
XM_011511957.1:c.1052C>G	XP_011510259.1:p.Pro351Arg
XR_923034.1:n.2031C>G
NM_031942.5:c.1133C>G MANE Select	NP_114148.3:p.Pro378Arg
NM_145810.3:c.896C>G	NP_665809.1:p.Pro299Arg