Canonical Allele Identifier: CA349330820

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231107C>T (hg19) ; chr2:g.173366379C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366379C>T , CM000664.2:g.173366379C>T	GRCh38
NC_000002.11:g.174231107C>T , CM000664.1:g.174231107C>T	GRCh37
NC_000002.10:g.173939353C>T	NCBI36
NG_047202.1:g.17363C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-771C>T	ENSP00000512251.1:n.799-771C>T
ENST00000695911.1:c.910C>T	ENSP00000512262.1:n.910C>T
ENST00000695912.1:c.1129C>T	ENSP00000512263.1:p.Pro377Ser
ENST00000695913.1:c.*1885C>T	ENSP00000512264.1:n.*1885C>T
ENST00000695914.1:c.892C>T	ENSP00000512265.1:p.Pro298Ser
ENST00000695918.1:n.360C>T
ENST00000306721.8:c.1132C>T MANE Select	ENSP00000306968.3:p.Pro378Ser
ENST00000306721.7:c.1132C>T	ENSP00000306968.3:p.Pro378Ser
ENST00000347703.7:c.895C>T	ENSP00000272789.4:p.Pro299Ser
ENST00000410019.3:c.769C>T	ENSP00000386833.3:p.Pro257Ser
ENST00000410101.7:c.1000C>T	ENSP00000386656.3:p.Pro334Ser
ENST00000467411.5:n.1769-771C>T
ENST00000496441.5:n.1886C>T
NM_031942.4:c.1132C>T	NP_114148.3:p.Pro378Ser
NM_145810.2:c.895C>T	NP_665809.1:p.Pro299Ser
XM_011511957.1:c.1051C>T	XP_011510259.1:p.Pro351Ser
XR_923034.1:n.2030C>T
NM_031942.5:c.1132C>T MANE Select	NP_114148.3:p.Pro378Ser
NM_145810.3:c.895C>T	NP_665809.1:p.Pro299Ser