Canonical Allele Identifier: CA349330798

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231103T>A (hg19) ; chr2:g.173366375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366375T>A , CM000664.2:g.173366375T>A	GRCh38
NC_000002.11:g.174231103T>A , CM000664.1:g.174231103T>A	GRCh37
NC_000002.10:g.173939349T>A	NCBI36
NG_047202.1:g.17359T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-775T>A	ENSP00000512251.1:n.799-775T>A
ENST00000695911.1:c.906T>A	ENSP00000512262.1:n.906T>A
ENST00000695912.1:c.1125T>A	ENSP00000512263.1:p.Cys375Ter
ENST00000695913.1:c.*1881T>A	ENSP00000512264.1:n.*1881T>A
ENST00000695914.1:c.888T>A	ENSP00000512265.1:p.Cys296Ter
ENST00000695918.1:n.356T>A
ENST00000306721.8:c.1128T>A MANE Select	ENSP00000306968.3:p.Cys376Ter
ENST00000306721.7:c.1128T>A	ENSP00000306968.3:p.Cys376Ter
ENST00000347703.7:c.891T>A	ENSP00000272789.4:p.Cys297Ter
ENST00000410019.3:c.765T>A	ENSP00000386833.3:p.Cys255Ter
ENST00000410101.7:c.996T>A	ENSP00000386656.3:p.Cys332Ter
ENST00000467411.5:n.1769-775T>A
ENST00000496441.5:n.1882T>A
NM_031942.4:c.1128T>A	NP_114148.3:p.Cys376Ter
NM_145810.2:c.891T>A	NP_665809.1:p.Cys297Ter
XM_011511957.1:c.1047T>A	XP_011510259.1:p.Cys349Ter
XR_923034.1:n.2026T>A
NM_031942.5:c.1128T>A MANE Select	NP_114148.3:p.Cys376Ter
NM_145810.3:c.891T>A	NP_665809.1:p.Cys297Ter