Canonical Allele Identifier: CA429810516

Gene: CDCA7

Linked Data

• dbSNP Id: rs1246106322
• gnomAD v2: 2-174231121-C-T
• gnomAD v4: 2-173366393-C-T
• COSMIC: COSM4459917
• MyVariant Identifiers: chr2:g.174231121C>T (hg19) ; chr2:g.173366393C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366393C>T , CM000664.2:g.173366393C>T	GRCh38
NC_000002.11:g.174231121C>T , CM000664.1:g.174231121C>T	GRCh37
NC_000002.10:g.173939367C>T	NCBI36
NG_047202.1:g.17377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-757C>T	ENSP00000512251.1:n.799-757C>T
ENST00000695911.1:c.924C>T	ENSP00000512262.1:n.924C>T
ENST00000695912.1:c.1143C>T	ENSP00000512263.1:p.Asn381=
ENST00000695913.1:c.*1899C>T	ENSP00000512264.1:n.*1899C>T
ENST00000695914.1:c.906C>T	ENSP00000512265.1:p.Asn302=
ENST00000695918.1:n.374C>T
ENST00000306721.8:c.1146C>T MANE Select	ENSP00000306968.3:p.Asn382=
ENST00000306721.7:c.1146C>T	ENSP00000306968.3:p.Asn382=
ENST00000347703.7:c.909C>T	ENSP00000272789.4:p.Asn303=
ENST00000410019.3:c.783C>T	ENSP00000386833.3:p.Asn261=
ENST00000410101.7:c.1014C>T	ENSP00000386656.3:p.Asn338=
ENST00000467411.5:n.1769-757C>T
ENST00000496441.5:n.1900C>T
NM_031942.4:c.1146C>T	NP_114148.3:p.Asn382=
NM_145810.2:c.909C>T	NP_665809.1:p.Asn303=
XM_011511957.1:c.1065C>T	XP_011510259.1:p.Asn355=
XR_923034.1:n.2044C>T
NM_031942.5:c.1146C>T MANE Select	NP_114148.3:p.Asn382=
NM_145810.3:c.909C>T	NP_665809.1:p.Asn303=