Canonical Allele Identifier: CA349330860

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366388-C-T
• MyVariant Identifiers: chr2:g.174231116C>T (hg19) ; chr2:g.173366388C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366388C>T , CM000664.2:g.173366388C>T	GRCh38
NC_000002.11:g.174231116C>T , CM000664.1:g.174231116C>T	GRCh37
NC_000002.10:g.173939362C>T	NCBI36
NG_047202.1:g.17372C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-762C>T	ENSP00000512251.1:n.799-762C>T
ENST00000695911.1:c.919C>T	ENSP00000512262.1:n.919C>T
ENST00000695912.1:c.1138C>T	ENSP00000512263.1:p.Arg380Ter
ENST00000695913.1:c.*1894C>T	ENSP00000512264.1:n.*1894C>T
ENST00000695914.1:c.901C>T	ENSP00000512265.1:p.Arg301Ter
ENST00000695918.1:n.369C>T
ENST00000306721.8:c.1141C>T MANE Select	ENSP00000306968.3:p.Arg381Ter
ENST00000306721.7:c.1141C>T	ENSP00000306968.3:p.Arg381Ter
ENST00000347703.7:c.904C>T	ENSP00000272789.4:p.Arg302Ter
ENST00000410019.3:c.778C>T	ENSP00000386833.3:p.Arg260Ter
ENST00000410101.7:c.1009C>T	ENSP00000386656.3:p.Arg337Ter
ENST00000467411.5:n.1769-762C>T
ENST00000496441.5:n.1895C>T
NM_031942.4:c.1141C>T	NP_114148.3:p.Arg381Ter
NM_145810.2:c.904C>T	NP_665809.1:p.Arg302Ter
XM_011511957.1:c.1060C>T	XP_011510259.1:p.Arg354Ter
XR_923034.1:n.2039C>T
NM_031942.5:c.1141C>T MANE Select	NP_114148.3:p.Arg381Ter
NM_145810.3:c.904C>T	NP_665809.1:p.Arg302Ter