Canonical Allele Identifier: CA349330440

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231033G>T (hg19) ; chr2:g.173366305G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366305G>T , CM000664.2:g.173366305G>T	GRCh38
NC_000002.11:g.174231033G>T , CM000664.1:g.174231033G>T	GRCh37
NC_000002.10:g.173939279G>T	NCBI36
NG_047202.1:g.17289G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+713G>T	ENSP00000512251.1:n.798+713G>T
ENST00000695911.1:c.836G>T	ENSP00000512262.1:n.836G>T
ENST00000695912.1:c.1055G>T	ENSP00000512263.1:p.Arg352Leu
ENST00000695913.1:c.*1811G>T	ENSP00000512264.1:n.*1811G>T
ENST00000695914.1:c.818G>T	ENSP00000512265.1:p.Arg273Leu
ENST00000695918.1:n.286G>T
ENST00000306721.8:c.1058G>T MANE Select	ENSP00000306968.3:p.Arg353Leu
ENST00000306721.7:c.1058G>T	ENSP00000306968.3:p.Arg353Leu
ENST00000347703.7:c.821G>T	ENSP00000272789.4:p.Arg274Leu
ENST00000410019.3:c.695G>T	ENSP00000386833.3:p.Arg232Leu
ENST00000410101.7:c.926G>T	ENSP00000386656.3:p.Arg309Leu
ENST00000467411.5:n.1768+713G>T
ENST00000496441.5:n.1812G>T
NM_031942.4:c.1058G>T	NP_114148.3:p.Arg353Leu
NM_145810.2:c.821G>T	NP_665809.1:p.Arg274Leu
XM_011511957.1:c.977G>T	XP_011510259.1:p.Arg326Leu
XR_923034.1:n.1956G>T
NM_031942.5:c.1058G>T MANE Select	NP_114148.3:p.Arg353Leu
NM_145810.3:c.821G>T	NP_665809.1:p.Arg274Leu