Canonical Allele Identifier: CA349330769

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231098T>A (hg19) ; chr2:g.173366370T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366370T>A , CM000664.2:g.173366370T>A	GRCh38
NC_000002.11:g.174231098T>A , CM000664.1:g.174231098T>A	GRCh37
NC_000002.10:g.173939344T>A	NCBI36
NG_047202.1:g.17354T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+778T>A	ENSP00000512251.1:n.798+778T>A
ENST00000695911.1:c.901T>A	ENSP00000512262.1:n.901T>A
ENST00000695912.1:c.1120T>A	ENSP00000512263.1:p.Phe374Ile
ENST00000695913.1:c.*1876T>A	ENSP00000512264.1:n.*1876T>A
ENST00000695914.1:c.883T>A	ENSP00000512265.1:p.Phe295Ile
ENST00000695918.1:n.351T>A
ENST00000306721.8:c.1123T>A MANE Select	ENSP00000306968.3:p.Phe375Ile
ENST00000306721.7:c.1123T>A	ENSP00000306968.3:p.Phe375Ile
ENST00000347703.7:c.886T>A	ENSP00000272789.4:p.Phe296Ile
ENST00000410019.3:c.760T>A	ENSP00000386833.3:p.Phe254Ile
ENST00000410101.7:c.991T>A	ENSP00000386656.3:p.Phe331Ile
ENST00000467411.5:n.1768+778T>A
ENST00000496441.5:n.1877T>A
NM_031942.4:c.1123T>A	NP_114148.3:p.Phe375Ile
NM_145810.2:c.886T>A	NP_665809.1:p.Phe296Ile
XM_011511957.1:c.1042T>A	XP_011510259.1:p.Phe348Ile
XR_923034.1:n.2021T>A
NM_031942.5:c.1123T>A MANE Select	NP_114148.3:p.Phe375Ile
NM_145810.3:c.886T>A	NP_665809.1:p.Phe296Ile