Canonical Allele Identifier: CA349330758

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231096A>C (hg19) ; chr2:g.173366368A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366368A>C , CM000664.2:g.173366368A>C	GRCh38
NC_000002.11:g.174231096A>C , CM000664.1:g.174231096A>C	GRCh37
NC_000002.10:g.173939342A>C	NCBI36
NG_047202.1:g.17352A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+776A>C	ENSP00000512251.1:n.798+776A>C
ENST00000695911.1:c.899A>C	ENSP00000512262.1:n.899A>C
ENST00000695912.1:c.1118A>C	ENSP00000512263.1:p.Gln373Pro
ENST00000695913.1:c.*1874A>C	ENSP00000512264.1:n.*1874A>C
ENST00000695914.1:c.881A>C	ENSP00000512265.1:p.Gln294Pro
ENST00000695918.1:n.349A>C
ENST00000306721.8:c.1121A>C MANE Select	ENSP00000306968.3:p.Gln374Pro
ENST00000306721.7:c.1121A>C	ENSP00000306968.3:p.Gln374Pro
ENST00000347703.7:c.884A>C	ENSP00000272789.4:p.Gln295Pro
ENST00000410019.3:c.758A>C	ENSP00000386833.3:p.Gln253Pro
ENST00000410101.7:c.989A>C	ENSP00000386656.3:p.Gln330Pro
ENST00000467411.5:n.1768+776A>C
ENST00000496441.5:n.1875A>C
NM_031942.4:c.1121A>C	NP_114148.3:p.Gln374Pro
NM_145810.2:c.884A>C	NP_665809.1:p.Gln295Pro
XM_011511957.1:c.1040A>C	XP_011510259.1:p.Gln347Pro
XR_923034.1:n.2019A>C
NM_031942.5:c.1121A>C MANE Select	NP_114148.3:p.Gln374Pro
NM_145810.3:c.884A>C	NP_665809.1:p.Gln295Pro