Canonical Allele Identifier: CA349330772

Gene: CDCA7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+778T>C	ENSP00000512251.1:n.798+778T>C
ENST00000695911.1:c.901T>C	ENSP00000512262.1:n.901T>C
ENST00000695912.1:c.1120T>C	ENSP00000512263.1:p.Phe374Leu
ENST00000695913.1:c.*1876T>C	ENSP00000512264.1:n.*1876T>C
ENST00000695914.1:c.883T>C	ENSP00000512265.1:p.Phe295Leu
ENST00000695918.1:n.351T>C
ENST00000306721.8:c.1123T>C MANE Select	ENSP00000306968.3:p.Phe375Leu
ENST00000306721.7:c.1123T>C	ENSP00000306968.3:p.Phe375Leu
ENST00000347703.7:c.886T>C	ENSP00000272789.4:p.Phe296Leu
ENST00000410019.3:c.760T>C	ENSP00000386833.3:p.Phe254Leu
ENST00000410101.7:c.991T>C	ENSP00000386656.3:p.Phe331Leu
ENST00000467411.5:n.1768+778T>C
ENST00000496441.5:n.1877T>C
NM_031942.4:c.1123T>C	NP_114148.3:p.Phe375Leu
NM_145810.2:c.886T>C	NP_665809.1:p.Phe296Leu
XM_011511957.1:c.1042T>C	XP_011510259.1:p.Phe348Leu
XR_923034.1:n.2021T>C
NM_031942.5:c.1123T>C MANE Select	NP_114148.3:p.Phe375Leu
NM_145810.3:c.886T>C	NP_665809.1:p.Phe296Leu