Canonical Allele Identifier: CA252656

Gene: CDC73

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130173G>A , CM000663.2:g.193130173G>A	GRCh38
NC_000001.10:g.193099303G>A , CM000663.1:g.193099303G>A	GRCh37
NC_000001.9:g.191365926G>A	NCBI36
NG_012691.1:g.13216G>A , LRG_507:g.13216G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.238-1G>A MANE Select	ENSP00000356405.4:n.238-1G>A
ENST00000635846.1:c.238-1G>A	ENSP00000490035.1:n.238-1G>A
ENST00000643006.1:c.238-1G>A	ENSP00000496633.1:n.238-1G>A
ENST00000643784.1:c.238-1G>A	ENSP00000494944.1:n.238-1G>A
ENST00000647662.1:n.139-1G>A
ENST00000648071.1:c.*214-1G>A	ENSP00000497513.1:n.*214-1G>A
ENST00000649606.1:n.251-1G>A
ENST00000649706.1:n.179-1G>A
ENST00000649895.1:n.456-1G>A
ENST00000650197.1:c.238-1G>A	ENSP00000496929.1:n.238-1G>A
ENST00000367435.3:c.238-1G>A	ENSP00000356405.3:n.238-1G>A
ENST00000482484.1:n.490-1G>A
NM_024529.4:c.238-1G>A , LRG_507t1:c.238-1G>A	NP_078805.3:n.238-1G>A
XM_006711537.2:c.238-1G>A	XP_006711600.1:n.238-1G>A
XR_241165.2:n.303+184C>T
XM_006711537.4:c.238-1G>A	XP_006711600.1:n.238-1G>A
NM_024529.5:c.238-1G>A MANE Select	NP_078805.3:n.238-1G>A