Canonical Allele Identifier: CA1583245902

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604023A= , CM000667.2:g.132604023A=	GRCh38
NC_000005.9:g.131939715A= , CM000667.1:g.131939715A=	GRCh37
NC_000005.8:g.131967614A=	NCBI36
NG_021151.1:g.52100A=
NG_021151.2:g.52047A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2501A= MANE Select	ENSP00000368100.4:p.Glu834=
ENST00000638452.2:c.2204A=	ENSP00000492349.2:p.Glu735=
ENST00000638504.1:n.2109A=
ENST00000638568.2:c.2204A=	ENSP00000491158.2:p.Glu735=
ENST00000639899.1:n.3020A=
ENST00000640655.2:c.2204A=	ENSP00000491596.2:p.Glu735=
ENST00000651160.1:c.*645A=	ENSP00000498829.1:n.*645A=
ENST00000651658.1:n.3044A=
ENST00000651723.1:c.*2584A=	ENSP00000498237.1:n.*2584A=
ENST00000652016.1:c.*718A=	ENSP00000498267.1:n.*718A=
ENST00000652485.1:c.2534A=	ENSP00000498973.1:p.Glu845=
ENST00000378823.7:c.2501A=	ENSP00000368100.4:p.Glu834=
ENST00000423956.5:c.*687A=	ENSP00000390971.1:n.*687A=
ENST00000533482.5:c.*2127A=	ENSP00000431225.1:n.*2127A=
NM_005732.3:c.2501A=	NP_005723.2:p.Glu834=
NM_005732.4:c.2501A= MANE Select	NP_005723.2:p.Glu834=