Canonical Allele Identifier: CA349331113

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231161G>T (hg19) ; chr2:g.173366433G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366433G>T , CM000664.2:g.173366433G>T	GRCh38
NC_000002.11:g.174231161G>T , CM000664.1:g.174231161G>T	GRCh37
NC_000002.10:g.173939407G>T	NCBI36
NG_047202.1:g.17417G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-717G>T	ENSP00000512251.1:n.799-717G>T
ENST00000695911.1:c.963+1G>T	ENSP00000512262.1:n.963+1G>T
ENST00000695912.1:c.1182+1G>T	ENSP00000512263.1:n.1182+1G>T
ENST00000695913.1:c.*1938+1G>T	ENSP00000512264.1:n.*1938+1G>T
ENST00000695914.1:c.945+1G>T	ENSP00000512265.1:n.945+1G>T
ENST00000695918.1:n.413+1G>T
ENST00000306721.8:c.1185+1G>T MANE Select	ENSP00000306968.3:n.1185+1G>T
ENST00000306721.7:c.1185+1G>T	ENSP00000306968.3:n.1185+1G>T
ENST00000347703.7:c.948+1G>T	ENSP00000272789.4:n.948+1G>T
ENST00000410019.3:c.822+1G>T	ENSP00000386833.3:n.822+1G>T
ENST00000410101.7:c.1053+1G>T	ENSP00000386656.3:n.1053+1G>T
ENST00000467411.5:n.1769-717G>T
ENST00000496441.5:n.1939+1G>T
NM_031942.4:c.1185+1G>T	NP_114148.3:n.1185+1G>T
NM_145810.2:c.948+1G>T	NP_665809.1:n.948+1G>T
XM_011511957.1:c.1104+1G>T	XP_011510259.1:n.1104+1G>T
XR_923034.1:n.2083+1G>T
NM_031942.5:c.1185+1G>T MANE Select	NP_114148.3:n.1185+1G>T
NM_145810.3:c.948+1G>T	NP_665809.1:n.948+1G>T