Canonical Allele Identifier: CA349330746

Gene: CDCA7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+773G>T	ENSP00000512251.1:n.798+773G>T
ENST00000695911.1:c.896G>T	ENSP00000512262.1:n.896G>T
ENST00000695912.1:c.1115G>T	ENSP00000512263.1:p.Gly372Val
ENST00000695913.1:c.*1871G>T	ENSP00000512264.1:n.*1871G>T
ENST00000695914.1:c.878G>T	ENSP00000512265.1:p.Gly293Val
ENST00000695918.1:n.346G>T
ENST00000306721.8:c.1118G>T MANE Select	ENSP00000306968.3:p.Gly373Val
ENST00000306721.7:c.1118G>T	ENSP00000306968.3:p.Gly373Val
ENST00000347703.7:c.881G>T	ENSP00000272789.4:p.Gly294Val
ENST00000410019.3:c.755G>T	ENSP00000386833.3:p.Gly252Val
ENST00000410101.7:c.986G>T	ENSP00000386656.3:p.Gly329Val
ENST00000467411.5:n.1768+773G>T
ENST00000496441.5:n.1872G>T
NM_031942.4:c.1118G>T	NP_114148.3:p.Gly373Val
NM_145810.2:c.881G>T	NP_665809.1:p.Gly294Val
XM_011511957.1:c.1037G>T	XP_011510259.1:p.Gly346Val
XR_923034.1:n.2016G>T
NM_031942.5:c.1118G>T MANE Select	NP_114148.3:p.Gly373Val
NM_145810.3:c.881G>T	NP_665809.1:p.Gly294Val