Canonical Allele Identifier: CA349330783

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231100C>G (hg19) ; chr2:g.173366372C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366372C>G , CM000664.2:g.173366372C>G	GRCh38
NC_000002.11:g.174231100C>G , CM000664.1:g.174231100C>G	GRCh37
NC_000002.10:g.173939346C>G	NCBI36
NG_047202.1:g.17356C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-778C>G	ENSP00000512251.1:n.799-778C>G
ENST00000695911.1:c.903C>G	ENSP00000512262.1:n.903C>G
ENST00000695912.1:c.1122C>G	ENSP00000512263.1:p.Phe374Leu
ENST00000695913.1:c.*1878C>G	ENSP00000512264.1:n.*1878C>G
ENST00000695914.1:c.885C>G	ENSP00000512265.1:p.Phe295Leu
ENST00000695918.1:n.353C>G
ENST00000306721.8:c.1125C>G MANE Select	ENSP00000306968.3:p.Phe375Leu
ENST00000306721.7:c.1125C>G	ENSP00000306968.3:p.Phe375Leu
ENST00000347703.7:c.888C>G	ENSP00000272789.4:p.Phe296Leu
ENST00000410019.3:c.762C>G	ENSP00000386833.3:p.Phe254Leu
ENST00000410101.7:c.993C>G	ENSP00000386656.3:p.Phe331Leu
ENST00000467411.5:n.1769-778C>G
ENST00000496441.5:n.1879C>G
NM_031942.4:c.1125C>G	NP_114148.3:p.Phe375Leu
NM_145810.2:c.888C>G	NP_665809.1:p.Phe296Leu
XM_011511957.1:c.1044C>G	XP_011510259.1:p.Phe348Leu
XR_923034.1:n.2023C>G
NM_031942.5:c.1125C>G MANE Select	NP_114148.3:p.Phe375Leu
NM_145810.3:c.888C>G	NP_665809.1:p.Phe296Leu