Canonical Allele Identifier: CA349330485

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231047G>T (hg19) ; chr2:g.173366319G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366319G>T , CM000664.2:g.173366319G>T	GRCh38
NC_000002.11:g.174231047G>T , CM000664.1:g.174231047G>T	GRCh37
NC_000002.10:g.173939293G>T	NCBI36
NG_047202.1:g.17303G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+727G>T	ENSP00000512251.1:n.798+727G>T
ENST00000695911.1:c.850G>T	ENSP00000512262.1:n.850G>T
ENST00000695912.1:c.1069G>T	ENSP00000512263.1:p.Asp357Tyr
ENST00000695913.1:c.*1825G>T	ENSP00000512264.1:n.*1825G>T
ENST00000695914.1:c.832G>T	ENSP00000512265.1:p.Asp278Tyr
ENST00000695918.1:n.300G>T
ENST00000306721.8:c.1072G>T MANE Select	ENSP00000306968.3:p.Asp358Tyr
ENST00000306721.7:c.1072G>T	ENSP00000306968.3:p.Asp358Tyr
ENST00000347703.7:c.835G>T	ENSP00000272789.4:p.Asp279Tyr
ENST00000410019.3:c.709G>T	ENSP00000386833.3:p.Asp237Tyr
ENST00000410101.7:c.940G>T	ENSP00000386656.3:p.Asp314Tyr
ENST00000467411.5:n.1768+727G>T
ENST00000496441.5:n.1826G>T
NM_031942.4:c.1072G>T	NP_114148.3:p.Asp358Tyr
NM_145810.2:c.835G>T	NP_665809.1:p.Asp279Tyr
XM_011511957.1:c.991G>T	XP_011510259.1:p.Asp331Tyr
XR_923034.1:n.1970G>T
NM_031942.5:c.1072G>T MANE Select	NP_114148.3:p.Asp358Tyr
NM_145810.3:c.835G>T	NP_665809.1:p.Asp279Tyr