Canonical Allele Identifier: CA349330450

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231036A>T (hg19) ; chr2:g.173366308A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366308A>T , CM000664.2:g.173366308A>T	GRCh38
NC_000002.11:g.174231036A>T , CM000664.1:g.174231036A>T	GRCh37
NC_000002.10:g.173939282A>T	NCBI36
NG_047202.1:g.17292A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+716A>T	ENSP00000512251.1:n.798+716A>T
ENST00000695911.1:c.839A>T	ENSP00000512262.1:n.839A>T
ENST00000695912.1:c.1058A>T	ENSP00000512263.1:p.Gln353Leu
ENST00000695913.1:c.*1814A>T	ENSP00000512264.1:n.*1814A>T
ENST00000695914.1:c.821A>T	ENSP00000512265.1:p.Gln274Leu
ENST00000695918.1:n.289A>T
ENST00000306721.8:c.1061A>T MANE Select	ENSP00000306968.3:p.Gln354Leu
ENST00000306721.7:c.1061A>T	ENSP00000306968.3:p.Gln354Leu
ENST00000347703.7:c.824A>T	ENSP00000272789.4:p.Gln275Leu
ENST00000410019.3:c.698A>T	ENSP00000386833.3:p.Gln233Leu
ENST00000410101.7:c.929A>T	ENSP00000386656.3:p.Gln310Leu
ENST00000467411.5:n.1768+716A>T
ENST00000496441.5:n.1815A>T
NM_031942.4:c.1061A>T	NP_114148.3:p.Gln354Leu
NM_145810.2:c.824A>T	NP_665809.1:p.Gln275Leu
XM_011511957.1:c.980A>T	XP_011510259.1:p.Gln327Leu
XR_923034.1:n.1959A>T
NM_031942.5:c.1061A>T MANE Select	NP_114148.3:p.Gln354Leu
NM_145810.3:c.824A>T	NP_665809.1:p.Gln275Leu