Canonical Allele Identifier: CA349330613

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366341-A-G
• MyVariant Identifiers: chr2:g.174231069A>G (hg19) ; chr2:g.173366341A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366341A>G , CM000664.2:g.173366341A>G	GRCh38
NC_000002.11:g.174231069A>G , CM000664.1:g.174231069A>G	GRCh37
NC_000002.10:g.173939315A>G	NCBI36
NG_047202.1:g.17325A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+749A>G	ENSP00000512251.1:n.798+749A>G
ENST00000695911.1:c.872A>G	ENSP00000512262.1:n.872A>G
ENST00000695912.1:c.1091A>G	ENSP00000512263.1:p.Asn364Ser
ENST00000695913.1:c.*1847A>G	ENSP00000512264.1:n.*1847A>G
ENST00000695914.1:c.854A>G	ENSP00000512265.1:p.Asn285Ser
ENST00000695918.1:n.322A>G
ENST00000306721.8:c.1094A>G MANE Select	ENSP00000306968.3:p.Asn365Ser
ENST00000306721.7:c.1094A>G	ENSP00000306968.3:p.Asn365Ser
ENST00000347703.7:c.857A>G	ENSP00000272789.4:p.Asn286Ser
ENST00000410019.3:c.731A>G	ENSP00000386833.3:p.Asn244Ser
ENST00000410101.7:c.962A>G	ENSP00000386656.3:p.Asn321Ser
ENST00000467411.5:n.1768+749A>G
ENST00000496441.5:n.1848A>G
NM_031942.4:c.1094A>G	NP_114148.3:p.Asn365Ser
NM_145810.2:c.857A>G	NP_665809.1:p.Asn286Ser
XM_011511957.1:c.1013A>G	XP_011510259.1:p.Asn338Ser
XR_923034.1:n.1992A>G
NM_031942.5:c.1094A>G MANE Select	NP_114148.3:p.Asn365Ser
NM_145810.3:c.857A>G	NP_665809.1:p.Asn286Ser