Canonical Allele Identifier: CA1583229571

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609171G= , CM000667.2:g.132609171G=	GRCh38
NC_000005.9:g.131944863G= , CM000667.1:g.131944863G=	GRCh37
NC_000005.8:g.131972762G=	NCBI36
NG_021151.1:g.57248G=
NG_021151.2:g.57195G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2884G= MANE Select	ENSP00000368100.4:p.Glu962=
ENST00000638452.2:c.2587G=	ENSP00000492349.2:p.Glu863=
ENST00000638504.1:n.2492G=
ENST00000638568.2:c.2587G=	ENSP00000491158.2:p.Glu863=
ENST00000639899.1:n.3403G=
ENST00000640655.2:c.2587G=	ENSP00000491596.2:p.Glu863=
ENST00000651160.1:c.*1028G=	ENSP00000498829.1:n.*1028G=
ENST00000651723.1:c.*2967G=	ENSP00000498237.1:n.*2967G=
ENST00000378823.7:c.2884G=	ENSP00000368100.4:p.Glu962=
ENST00000423956.5:c.*1070G=	ENSP00000390971.1:n.*1070G=
ENST00000533482.5:c.*2510G=	ENSP00000431225.1:n.*2510G=
NM_005732.3:c.2884G=	NP_005723.2:p.Glu962=
NM_005732.4:c.2884G= MANE Select	NP_005723.2:p.Glu962=