Canonical Allele Identifier: CA429810507

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231109C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366381C>T , CM000664.2:g.173366381C>T	GRCh38
NC_000002.11:g.174231109C>T , CM000664.1:g.174231109C>T	GRCh37
NC_000002.10:g.173939355C>T	NCBI36
NG_047202.1:g.17365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-769C>T	ENSP00000512251.1:n.799-769C>T
ENST00000695911.1:c.912C>T	ENSP00000512262.1:n.912C>T
ENST00000695912.1:c.1131C>T	ENSP00000512263.1:p.Pro377=
ENST00000695913.1:c.*1887C>T	ENSP00000512264.1:n.*1887C>T
ENST00000695914.1:c.894C>T	ENSP00000512265.1:p.Pro298=
ENST00000695918.1:n.362C>T
ENST00000306721.8:c.1134C>T MANE Select	ENSP00000306968.3:p.Pro378=
ENST00000306721.7:c.1134C>T	ENSP00000306968.3:p.Pro378=
ENST00000347703.7:c.897C>T	ENSP00000272789.4:p.Pro299=
ENST00000410019.3:c.771C>T	ENSP00000386833.3:p.Pro257=
ENST00000410101.7:c.1002C>T	ENSP00000386656.3:p.Pro334=
ENST00000467411.5:n.1769-769C>T
ENST00000496441.5:n.1888C>T
NM_031942.4:c.1134C>T	NP_114148.3:p.Pro378=
NM_145810.2:c.897C>T	NP_665809.1:p.Pro299=
XM_011511957.1:c.1053C>T	XP_011510259.1:p.Pro351=
XR_923034.1:n.2032C>T
NM_031942.5:c.1134C>T MANE Select	NP_114148.3:p.Pro378=
NM_145810.3:c.897C>T	NP_665809.1:p.Pro299=