Canonical Allele Identifier: CA429810538

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231154G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366426G>C , CM000664.2:g.173366426G>C	GRCh38
NC_000002.11:g.174231154G>C , CM000664.1:g.174231154G>C	GRCh37
NC_000002.10:g.173939400G>C	NCBI36
NG_047202.1:g.17410G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-724G>C	ENSP00000512251.1:n.799-724G>C
ENST00000695911.1:c.957G>C	ENSP00000512262.1:n.957G>C
ENST00000695912.1:c.1176G>C	ENSP00000512263.1:p.Leu392=
ENST00000695913.1:c.*1932G>C	ENSP00000512264.1:n.*1932G>C
ENST00000695914.1:c.939G>C	ENSP00000512265.1:p.Leu313=
ENST00000695918.1:n.407G>C
ENST00000306721.8:c.1179G>C MANE Select	ENSP00000306968.3:p.Leu393=
ENST00000306721.7:c.1179G>C	ENSP00000306968.3:p.Leu393=
ENST00000347703.7:c.942G>C	ENSP00000272789.4:p.Leu314=
ENST00000410019.3:c.816G>C	ENSP00000386833.3:p.Leu272=
ENST00000410101.7:c.1047G>C	ENSP00000386656.3:p.Leu349=
ENST00000467411.5:n.1769-724G>C
ENST00000496441.5:n.1933G>C
NM_031942.4:c.1179G>C	NP_114148.3:p.Leu393=
NM_145810.2:c.942G>C	NP_665809.1:p.Leu314=
XM_011511957.1:c.1098G>C	XP_011510259.1:p.Leu366=
XR_923034.1:n.2077G>C
NM_031942.5:c.1179G>C MANE Select	NP_114148.3:p.Leu393=
NM_145810.3:c.942G>C	NP_665809.1:p.Leu314=