Canonical Allele Identifier: CA2768436990

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604126_132604127insTT , CM000667.2:g.132604126_132604127insTT	GRCh38
NC_000005.9:g.131939818_131939819insTT , CM000667.1:g.131939818_131939819insTT	GRCh37
NC_000005.8:g.131967717_131967718insTT	NCBI36
NG_021151.1:g.52203_52204insTT
NG_021151.2:g.52150_52151insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2524+80_2524+81insTT MANE Select	ENSP00000368100.4:n.2524+80_2524+81insTT
ENST00000638452.2:c.2227+80_2227+81insTT	ENSP00000492349.2:n.2227+80_2227+81insTT
ENST00000638504.1:n.2132+80_2132+81insTT
ENST00000638568.2:c.2227+80_2227+81insTT	ENSP00000491158.2:n.2227+80_2227+81insTT
ENST00000639899.1:n.3043+80_3043+81insTT
ENST00000640655.2:c.2227+80_2227+81insTT	ENSP00000491596.2:n.2227+80_2227+81insTT
ENST00000651160.1:c.*668+80_*668+81insTT	ENSP00000498829.1:n.*668+80_*668+81insTT
ENST00000651723.1:c.*2607+80_*2607+81insTT	ENSP00000498237.1:n.*2607+80_*2607+81insTT
ENST00000652016.1:c.*741+80_*741+81insTT	ENSP00000498267.1:n.*741+80_*741+81insTT
ENST00000652485.1:c.2557+80_2557+81insTT	ENSP00000498973.1:n.2557+80_2557+81insTT
ENST00000378823.7:c.2524+80_2524+81insTT	ENSP00000368100.4:n.2524+80_2524+81insTT
ENST00000423956.5:c.*710+80_*710+81insTT	ENSP00000390971.1:n.*710+80_*710+81insTT
ENST00000533482.5:c.*2150+80_*2150+81insTT	ENSP00000431225.1:n.*2150+80_*2150+81insTT
NM_005732.3:c.2524+80_2524+81insTT	NP_005723.2:n.2524+80_2524+81insTT
NM_005732.4:c.2524+80_2524+81insTT MANE Select	NP_005723.2:n.2524+80_2524+81insTT