Canonical Allele Identifier: CA349330792

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231102G>A (hg19) ; chr2:g.173366374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366374G>A , CM000664.2:g.173366374G>A	GRCh38
NC_000002.11:g.174231102G>A , CM000664.1:g.174231102G>A	GRCh37
NC_000002.10:g.173939348G>A	NCBI36
NG_047202.1:g.17358G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-776G>A	ENSP00000512251.1:n.799-776G>A
ENST00000695911.1:c.905G>A	ENSP00000512262.1:n.905G>A
ENST00000695912.1:c.1124G>A	ENSP00000512263.1:p.Cys375Tyr
ENST00000695913.1:c.*1880G>A	ENSP00000512264.1:n.*1880G>A
ENST00000695914.1:c.887G>A	ENSP00000512265.1:p.Cys296Tyr
ENST00000695918.1:n.355G>A
ENST00000306721.8:c.1127G>A MANE Select	ENSP00000306968.3:p.Cys376Tyr
ENST00000306721.7:c.1127G>A	ENSP00000306968.3:p.Cys376Tyr
ENST00000347703.7:c.890G>A	ENSP00000272789.4:p.Cys297Tyr
ENST00000410019.3:c.764G>A	ENSP00000386833.3:p.Cys255Tyr
ENST00000410101.7:c.995G>A	ENSP00000386656.3:p.Cys332Tyr
ENST00000467411.5:n.1769-776G>A
ENST00000496441.5:n.1881G>A
NM_031942.4:c.1127G>A	NP_114148.3:p.Cys376Tyr
NM_145810.2:c.890G>A	NP_665809.1:p.Cys297Tyr
XM_011511957.1:c.1046G>A	XP_011510259.1:p.Cys349Tyr
XR_923034.1:n.2025G>A
NM_031942.5:c.1127G>A MANE Select	NP_114148.3:p.Cys376Tyr
NM_145810.3:c.890G>A	NP_665809.1:p.Cys297Tyr