Canonical Allele Identifier: CA422351274

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130188T>A , CM000663.2:g.193130188T>A	GRCh38
NC_000001.10:g.193099318T>A , CM000663.1:g.193099318T>A	GRCh37
NC_000001.9:g.191365941T>A	NCBI36
NG_012691.1:g.13231T>A , LRG_507:g.13231T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.252T>A MANE Select	NP_078805.3:p.Pro84=
ENST00000367435.5:c.252T>A MANE Select	ENSP00000356405.4:p.Pro84=
NM_024529.4:c.252T>A , LRG_507t1:c.252T>A	NP_078805.3:p.Pro84=
ENST00000367435.3:c.252T>A	ENSP00000356405.3:p.Pro84=
ENST00000482484.1:n.504T>A
ENST00000635846.1:c.252T>A	ENSP00000490035.1:p.Pro84=
ENST00000643006.1:c.252T>A	ENSP00000496633.1:p.Pro84=
ENST00000643784.1:c.252T>A	ENSP00000494944.1:p.Pro84=
ENST00000647662.1:n.153T>A
ENST00000648071.1:c.*228T>A	ENSP00000497513.1:n.*228T>A
ENST00000649606.1:n.265T>A
ENST00000649706.1:n.193T>A
ENST00000649895.1:n.470T>A
ENST00000650197.1:c.252T>A	ENSP00000496929.1:p.Pro84=
XM_006711537.2:c.252T>A	XP_006711600.1:p.Pro84=
XM_006711537.4:c.252T>A	XP_006711600.1:p.Pro84=
XR_241165.2:n.303+169A>T