Canonical Allele Identifier: CA2838212614

Gene: RAD9A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67395898T>A , CM000673.2:g.67395898T>A	GRCh38
NC_000011.9:g.67163369T>A , CM000673.1:g.67163369T>A	GRCh37
NC_000011.8:g.66919945T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307980.7:c.560-14T>A MANE Select	ENSP00000311360.2:n.560-14T>A
ENST00000307980.6:c.560-14T>A	ENSP00000311360.2:n.560-14T>A
ENST00000529100.5:n.517-14T>A
ENST00000530934.5:n.940-14T>A
ENST00000535644.1:n.157-14T>A
ENST00000538013.5:c.*129-14T>A	ENSP00000442064.1:n.*129-14T>A
ENST00000543808.5:n.712-14T>A
ENST00000544620.5:c.518-14T>A	ENSP00000444979.1:n.518-14T>A
NM_001243224.1:c.332-14T>A	NP_001230153.1:n.332-14T>A
NM_004584.2:c.560-14T>A	NP_004575.1:n.560-14T>A
XM_006718652.2:c.593-14T>A	XP_006718715.1:n.593-14T>A
XM_011545205.1:c.-17-14T>A	XP_011543507.1:n.-17-14T>A
XR_428922.2:n.867-14T>A
XM_006718652.3:c.593-14T>A	XP_006718715.1:n.593-14T>A
XM_017018097.1:c.224-14T>A	XP_016873586.1:n.224-14T>A
XM_017018098.1:c.-17-14T>A	XP_016873587.1:n.-17-14T>A
XR_428922.3:n.867-14T>A
NM_004584.3:c.560-14T>A MANE Select	NP_004575.1:n.560-14T>A