Canonical Allele Identifier: CA349330744

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231093G>C (hg19) ; chr2:g.173366365G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366365G>C , CM000664.2:g.173366365G>C	GRCh38
NC_000002.11:g.174231093G>C , CM000664.1:g.174231093G>C	GRCh37
NC_000002.10:g.173939339G>C	NCBI36
NG_047202.1:g.17349G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+773G>C	ENSP00000512251.1:n.798+773G>C
ENST00000695911.1:c.896G>C	ENSP00000512262.1:n.896G>C
ENST00000695912.1:c.1115G>C	ENSP00000512263.1:p.Gly372Ala
ENST00000695913.1:c.*1871G>C	ENSP00000512264.1:n.*1871G>C
ENST00000695914.1:c.878G>C	ENSP00000512265.1:p.Gly293Ala
ENST00000695918.1:n.346G>C
ENST00000306721.8:c.1118G>C MANE Select	ENSP00000306968.3:p.Gly373Ala
ENST00000306721.7:c.1118G>C	ENSP00000306968.3:p.Gly373Ala
ENST00000347703.7:c.881G>C	ENSP00000272789.4:p.Gly294Ala
ENST00000410019.3:c.755G>C	ENSP00000386833.3:p.Gly252Ala
ENST00000410101.7:c.986G>C	ENSP00000386656.3:p.Gly329Ala
ENST00000467411.5:n.1768+773G>C
ENST00000496441.5:n.1872G>C
NM_031942.4:c.1118G>C	NP_114148.3:p.Gly373Ala
NM_145810.2:c.881G>C	NP_665809.1:p.Gly294Ala
XM_011511957.1:c.1037G>C	XP_011510259.1:p.Gly346Ala
XR_923034.1:n.2016G>C
NM_031942.5:c.1118G>C MANE Select	NP_114148.3:p.Gly373Ala
NM_145810.3:c.881G>C	NP_665809.1:p.Gly294Ala