Canonical Allele Identifier: CA349330693

Gene: CDCA7

Linked Data

• dbSNP Id: rs1246798003
• gnomAD v2: 2-174231082-G-A
• gnomAD v4: 2-173366354-G-A
• MyVariant Identifiers: chr2:g.174231082G>A (hg19) ; chr2:g.173366354G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366354G>A , CM000664.2:g.173366354G>A	GRCh38
NC_000002.11:g.174231082G>A , CM000664.1:g.174231082G>A	GRCh37
NC_000002.10:g.173939328G>A	NCBI36
NG_047202.1:g.17338G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+762G>A	ENSP00000512251.1:n.798+762G>A
ENST00000695911.1:c.885G>A	ENSP00000512262.1:n.885G>A
ENST00000695912.1:c.1104G>A	ENSP00000512263.1:p.Trp368Ter
ENST00000695913.1:c.*1860G>A	ENSP00000512264.1:n.*1860G>A
ENST00000695914.1:c.867G>A	ENSP00000512265.1:p.Trp289Ter
ENST00000695918.1:n.335G>A
ENST00000306721.8:c.1107G>A MANE Select	ENSP00000306968.3:p.Trp369Ter
ENST00000306721.7:c.1107G>A	ENSP00000306968.3:p.Trp369Ter
ENST00000347703.7:c.870G>A	ENSP00000272789.4:p.Trp290Ter
ENST00000410019.3:c.744G>A	ENSP00000386833.3:p.Trp248Ter
ENST00000410101.7:c.975G>A	ENSP00000386656.3:p.Trp325Ter
ENST00000467411.5:n.1768+762G>A
ENST00000496441.5:n.1861G>A
NM_031942.4:c.1107G>A	NP_114148.3:p.Trp369Ter
NM_145810.2:c.870G>A	NP_665809.1:p.Trp290Ter
XM_011511957.1:c.1026G>A	XP_011510259.1:p.Trp342Ter
XR_923034.1:n.2005G>A
NM_031942.5:c.1107G>A MANE Select	NP_114148.3:p.Trp369Ter
NM_145810.3:c.870G>A	NP_665809.1:p.Trp290Ter