Canonical Allele Identifier: CA349330883

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366393-C-G
• MyVariant Identifiers: chr2:g.174231121C>G (hg19) ; chr2:g.173366393C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-757C>G	ENSP00000512251.1:n.799-757C>G
ENST00000695911.1:c.924C>G	ENSP00000512262.1:n.924C>G
ENST00000695912.1:c.1143C>G	ENSP00000512263.1:p.Asn381Lys
ENST00000695913.1:c.*1899C>G	ENSP00000512264.1:n.*1899C>G
ENST00000695914.1:c.906C>G	ENSP00000512265.1:p.Asn302Lys
ENST00000695918.1:n.374C>G
ENST00000306721.8:c.1146C>G MANE Select	ENSP00000306968.3:p.Asn382Lys
ENST00000306721.7:c.1146C>G	ENSP00000306968.3:p.Asn382Lys
ENST00000347703.7:c.909C>G	ENSP00000272789.4:p.Asn303Lys
ENST00000410019.3:c.783C>G	ENSP00000386833.3:p.Asn261Lys
ENST00000410101.7:c.1014C>G	ENSP00000386656.3:p.Asn338Lys
ENST00000467411.5:n.1769-757C>G
ENST00000496441.5:n.1900C>G
NM_031942.4:c.1146C>G	NP_114148.3:p.Asn382Lys
NM_145810.2:c.909C>G	NP_665809.1:p.Asn303Lys
XM_011511957.1:c.1065C>G	XP_011510259.1:p.Asn355Lys
XR_923034.1:n.2044C>G
NM_031942.5:c.1146C>G MANE Select	NP_114148.3:p.Asn382Lys
NM_145810.3:c.909C>G	NP_665809.1:p.Asn303Lys