Canonical Allele Identifier: CA1583229599

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609220A= , CM000667.2:g.132609220A=	GRCh38
NC_000005.9:g.131944912A= , CM000667.1:g.131944912A=	GRCh37
NC_000005.8:g.131972811A=	NCBI36
NG_021151.1:g.57297A=
NG_021151.2:g.57244A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2922+11A= MANE Select	ENSP00000368100.4:n.2922+11A=
ENST00000638452.2:c.2625+11A=	ENSP00000492349.2:n.2625+11A=
ENST00000638504.1:n.2530+11A=
ENST00000638568.2:c.2625+11A=	ENSP00000491158.2:n.2625+11A=
ENST00000639899.1:n.3441+11A=
ENST00000640655.2:c.2625+11A=	ENSP00000491596.2:n.2625+11A=
ENST00000651160.1:c.*1066+11A=	ENSP00000498829.1:n.*1066+11A=
ENST00000651723.1:c.*3005+11A=	ENSP00000498237.1:n.*3005+11A=
ENST00000378823.7:c.2922+11A=	ENSP00000368100.4:n.2922+11A=
ENST00000423956.5:c.*1108+11A=	ENSP00000390971.1:n.*1108+11A=
ENST00000533482.5:c.*2548+11A=	ENSP00000431225.1:n.*2548+11A=
NM_005732.3:c.2922+11A=	NP_005723.2:n.2922+11A=
NM_005732.4:c.2922+11A= MANE Select	NP_005723.2:n.2922+11A=