Canonical Allele Identifier: CA1583254579

Gene: RAD50 TH2LCRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132642203_132642204delinsCG , CM000667.2:g.132642203_132642204delinsCG	GRCh38
NC_000005.9:g.131977895_131977896delinsCG , CM000667.1:g.131977895_131977896delinsCG	GRCh37
NC_000005.8:g.132005794_132005795delinsCG	NCBI36
NG_021151.1:g.90280_90281delinsCG
NG_021151.2:g.90227_90228delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3778_3779delinsCG (RAD50) MANE Select	ENSP00000368100.4:p.Arg1260=
ENST00000638452.2:c.3481_3482delinsCG	ENSP00000492349.2:p.Arg1161=
ENST00000638504.1:n.3386_3387delinsCG
ENST00000638568.2:c.3481_3482delinsCG	ENSP00000491158.2:p.Arg1161=
ENST00000639899.1:n.4297_4298delinsCG
ENST00000640655.2:c.3481_3482delinsCG	ENSP00000491596.2:p.Arg1161=
ENST00000651249.1:c.614_615delinsCG (RAD50)
ENST00000378823.7:c.3778_3779delinsCG (RAD50)	ENSP00000368100.4:p.Arg1260=
ENST00000455677.1:c.388-802_388-801delinsCG (RAD50)
ENST00000533482.5:c.*3404_*3405delinsCG (RAD50)	ENSP00000431225.1:n.*3404_*3405delinsCG
NM_005732.3:c.3778_3779delinsCG (RAD50)	NP_005723.2:p.Arg1260=
NR_132125.1:n.183_184delinsCG (TH2LCRR)
NR_132126.1:n.175-3939_175-3938delinsCG (TH2LCRR)
NM_005732.4:c.3778_3779delinsCG (RAD50) MANE Select	NP_005723.2:p.Arg1260=