Canonical Allele Identifier: CA349330754

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231095C>T (hg19) ; chr2:g.173366367C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366367C>T , CM000664.2:g.173366367C>T	GRCh38
NC_000002.11:g.174231095C>T , CM000664.1:g.174231095C>T	GRCh37
NC_000002.10:g.173939341C>T	NCBI36
NG_047202.1:g.17351C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+775C>T	ENSP00000512251.1:n.798+775C>T
ENST00000695911.1:c.898C>T	ENSP00000512262.1:n.898C>T
ENST00000695912.1:c.1117C>T	ENSP00000512263.1:p.Gln373Ter
ENST00000695913.1:c.*1873C>T	ENSP00000512264.1:n.*1873C>T
ENST00000695914.1:c.880C>T	ENSP00000512265.1:p.Gln294Ter
ENST00000695918.1:n.348C>T
ENST00000306721.8:c.1120C>T MANE Select	ENSP00000306968.3:p.Gln374Ter
ENST00000306721.7:c.1120C>T	ENSP00000306968.3:p.Gln374Ter
ENST00000347703.7:c.883C>T	ENSP00000272789.4:p.Gln295Ter
ENST00000410019.3:c.757C>T	ENSP00000386833.3:p.Gln253Ter
ENST00000410101.7:c.988C>T	ENSP00000386656.3:p.Gln330Ter
ENST00000467411.5:n.1768+775C>T
ENST00000496441.5:n.1874C>T
NM_031942.4:c.1120C>T	NP_114148.3:p.Gln374Ter
NM_145810.2:c.883C>T	NP_665809.1:p.Gln295Ter
XM_011511957.1:c.1039C>T	XP_011510259.1:p.Gln347Ter
XR_923034.1:n.2018C>T
NM_031942.5:c.1120C>T MANE Select	NP_114148.3:p.Gln374Ter
NM_145810.3:c.883C>T	NP_665809.1:p.Gln295Ter