Canonical Allele Identifier: CA1583238283

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588842A= , CM000667.2:g.132588842A=	GRCh38
NC_000005.9:g.131924534A= , CM000667.1:g.131924534A=	GRCh37
NC_000005.8:g.131952433A=	NCBI36
NG_021151.1:g.36919A=
NG_021151.2:g.36866A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1207A= MANE Select	ENSP00000368100.4:p.Arg403=
ENST00000638452.2:c.910A=	ENSP00000492349.2:p.Arg304=
ENST00000638504.1:n.893A=
ENST00000638568.2:c.910A=	ENSP00000491158.2:p.Arg304=
ENST00000639899.1:n.1726A=
ENST00000640655.2:c.910A=	ENSP00000491596.2:p.Arg304=
ENST00000651160.1:c.1207A=	ENSP00000498829.1:p.Arg403=
ENST00000651541.1:c.910A=	ENSP00000498795.1:p.Arg304=
ENST00000651658.1:n.1634A=
ENST00000651723.1:c.*1290A=	ENSP00000498237.1:n.*1290A=
ENST00000652016.1:c.1207A=	ENSP00000498267.1:p.Arg403=
ENST00000652485.1:c.1207A=	ENSP00000498973.1:p.Arg403=
ENST00000378823.7:c.1207A=	ENSP00000368100.4:p.Arg403=
ENST00000423956.5:c.1207A=	ENSP00000390971.1:p.Arg403=
ENST00000453394.5:c.1207A=	ENSP00000400049.1:p.Arg403=
ENST00000533482.5:c.*833A=	ENSP00000431225.1:n.*833A=
NM_005732.3:c.1207A=	NP_005723.2:p.Arg403=
NM_005732.4:c.1207A= MANE Select	NP_005723.2:p.Arg403=