Canonical Allele Identifier: CA349330671

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231079C>A (hg19) ; chr2:g.173366351C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366351C>A , CM000664.2:g.173366351C>A	GRCh38
NC_000002.11:g.174231079C>A , CM000664.1:g.174231079C>A	GRCh37
NC_000002.10:g.173939325C>A	NCBI36
NG_047202.1:g.17335C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+759C>A	ENSP00000512251.1:n.798+759C>A
ENST00000695911.1:c.882C>A	ENSP00000512262.1:n.882C>A
ENST00000695912.1:c.1101C>A	ENSP00000512263.1:p.Cys367Ter
ENST00000695913.1:c.*1857C>A	ENSP00000512264.1:n.*1857C>A
ENST00000695914.1:c.864C>A	ENSP00000512265.1:p.Cys288Ter
ENST00000695918.1:n.332C>A
ENST00000306721.8:c.1104C>A MANE Select	ENSP00000306968.3:p.Cys368Ter
ENST00000306721.7:c.1104C>A	ENSP00000306968.3:p.Cys368Ter
ENST00000347703.7:c.867C>A	ENSP00000272789.4:p.Cys289Ter
ENST00000410019.3:c.741C>A	ENSP00000386833.3:p.Cys247Ter
ENST00000410101.7:c.972C>A	ENSP00000386656.3:p.Cys324Ter
ENST00000467411.5:n.1768+759C>A
ENST00000496441.5:n.1858C>A
NM_031942.4:c.1104C>A	NP_114148.3:p.Cys368Ter
NM_145810.2:c.867C>A	NP_665809.1:p.Cys289Ter
XM_011511957.1:c.1023C>A	XP_011510259.1:p.Cys341Ter
XR_923034.1:n.2002C>A
NM_031942.5:c.1104C>A MANE Select	NP_114148.3:p.Cys368Ter
NM_145810.3:c.867C>A	NP_665809.1:p.Cys289Ter