Canonical Allele Identifier: CA349330470

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231041A>T (hg19) ; chr2:g.173366313A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366313A>T , CM000664.2:g.173366313A>T	GRCh38
NC_000002.11:g.174231041A>T , CM000664.1:g.174231041A>T	GRCh37
NC_000002.10:g.173939287A>T	NCBI36
NG_047202.1:g.17297A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+721A>T	ENSP00000512251.1:n.798+721A>T
ENST00000695911.1:c.844A>T	ENSP00000512262.1:n.844A>T
ENST00000695912.1:c.1063A>T	ENSP00000512263.1:p.Thr355Ser
ENST00000695913.1:c.*1819A>T	ENSP00000512264.1:n.*1819A>T
ENST00000695914.1:c.826A>T	ENSP00000512265.1:p.Thr276Ser
ENST00000695918.1:n.294A>T
ENST00000306721.8:c.1066A>T MANE Select	ENSP00000306968.3:p.Thr356Ser
ENST00000306721.7:c.1066A>T	ENSP00000306968.3:p.Thr356Ser
ENST00000347703.7:c.829A>T	ENSP00000272789.4:p.Thr277Ser
ENST00000410019.3:c.703A>T	ENSP00000386833.3:p.Thr235Ser
ENST00000410101.7:c.934A>T	ENSP00000386656.3:p.Thr312Ser
ENST00000467411.5:n.1768+721A>T
ENST00000496441.5:n.1820A>T
NM_031942.4:c.1066A>T	NP_114148.3:p.Thr356Ser
NM_145810.2:c.829A>T	NP_665809.1:p.Thr277Ser
XM_011511957.1:c.985A>T	XP_011510259.1:p.Thr329Ser
XR_923034.1:n.1964A>T
NM_031942.5:c.1066A>T MANE Select	NP_114148.3:p.Thr356Ser
NM_145810.3:c.829A>T	NP_665809.1:p.Thr277Ser