Canonical Allele Identifier: CA349330573

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366334-T-A
• MyVariant Identifiers: chr2:g.174231062T>A (hg19) ; chr2:g.173366334T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366334T>A , CM000664.2:g.173366334T>A	GRCh38
NC_000002.11:g.174231062T>A , CM000664.1:g.174231062T>A	GRCh37
NC_000002.10:g.173939308T>A	NCBI36
NG_047202.1:g.17318T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+742T>A	ENSP00000512251.1:n.798+742T>A
ENST00000695911.1:c.865T>A	ENSP00000512262.1:n.865T>A
ENST00000695912.1:c.1084T>A	ENSP00000512263.1:p.Cys362Ser
ENST00000695913.1:c.*1840T>A	ENSP00000512264.1:n.*1840T>A
ENST00000695914.1:c.847T>A	ENSP00000512265.1:p.Cys283Ser
ENST00000695918.1:n.315T>A
ENST00000306721.8:c.1087T>A MANE Select	ENSP00000306968.3:p.Cys363Ser
ENST00000306721.7:c.1087T>A	ENSP00000306968.3:p.Cys363Ser
ENST00000347703.7:c.850T>A	ENSP00000272789.4:p.Cys284Ser
ENST00000410019.3:c.724T>A	ENSP00000386833.3:p.Cys242Ser
ENST00000410101.7:c.955T>A	ENSP00000386656.3:p.Cys319Ser
ENST00000467411.5:n.1768+742T>A
ENST00000496441.5:n.1841T>A
NM_031942.4:c.1087T>A	NP_114148.3:p.Cys363Ser
NM_145810.2:c.850T>A	NP_665809.1:p.Cys284Ser
XM_011511957.1:c.1006T>A	XP_011510259.1:p.Cys336Ser
XR_923034.1:n.1985T>A
NM_031942.5:c.1087T>A MANE Select	NP_114148.3:p.Cys363Ser
NM_145810.3:c.850T>A	NP_665809.1:p.Cys284Ser