Canonical Allele Identifier: CA349330452

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231037G>C (hg19) ; chr2:g.173366309G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366309G>C , CM000664.2:g.173366309G>C	GRCh38
NC_000002.11:g.174231037G>C , CM000664.1:g.174231037G>C	GRCh37
NC_000002.10:g.173939283G>C	NCBI36
NG_047202.1:g.17293G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+717G>C	ENSP00000512251.1:n.798+717G>C
ENST00000695911.1:c.840G>C	ENSP00000512262.1:n.840G>C
ENST00000695912.1:c.1059G>C	ENSP00000512263.1:p.Gln353His
ENST00000695913.1:c.*1815G>C	ENSP00000512264.1:n.*1815G>C
ENST00000695914.1:c.822G>C	ENSP00000512265.1:p.Gln274His
ENST00000695918.1:n.290G>C
ENST00000306721.8:c.1062G>C MANE Select	ENSP00000306968.3:p.Gln354His
ENST00000306721.7:c.1062G>C	ENSP00000306968.3:p.Gln354His
ENST00000347703.7:c.825G>C	ENSP00000272789.4:p.Gln275His
ENST00000410019.3:c.699G>C	ENSP00000386833.3:p.Gln233His
ENST00000410101.7:c.930G>C	ENSP00000386656.3:p.Gln310His
ENST00000467411.5:n.1768+717G>C
ENST00000496441.5:n.1816G>C
NM_031942.4:c.1062G>C	NP_114148.3:p.Gln354His
NM_145810.2:c.825G>C	NP_665809.1:p.Gln275His
XM_011511957.1:c.981G>C	XP_011510259.1:p.Gln327His
XR_923034.1:n.1960G>C
NM_031942.5:c.1062G>C MANE Select	NP_114148.3:p.Gln354His
NM_145810.3:c.825G>C	NP_665809.1:p.Gln275His