Canonical Allele Identifier: CA650290459

Gene: RAD50 TH2LCRR

Linked Data

• COSMIC: COSN23845651

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132634073del , CM000667.2:g.132634073del	GRCh38
NC_000005.9:g.131969765del , CM000667.1:g.131969765del	GRCh37
NC_000005.8:g.131997664del	NCBI36
NG_021151.1:g.82150del
NG_021151.2:g.82097del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3390-3042del (RAD50) MANE Select	ENSP00000368100.4:n.3390-3042del
ENST00000638452.2:c.3093-3042del	ENSP00000492349.2:n.3093-3042del
ENST00000638504.1:n.2998-3042del
ENST00000638568.2:c.3093-3042del	ENSP00000491158.2:n.3093-3042del
ENST00000639899.1:n.3909-3042del
ENST00000640655.2:c.3093-3042del	ENSP00000491596.2:n.3093-3042del
ENST00000651249.1:c.226-3042del (RAD50)
ENST00000378823.7:c.3390-3042del (RAD50)	ENSP00000368100.4:n.3390-3042del
ENST00000455677.1:c.25-3042del (RAD50)
ENST00000533482.5:c.*3016-3042del (RAD50)	ENSP00000431225.1:n.*3016-3042del
NM_005732.3:c.3390-3042del (RAD50)	NP_005723.2:n.3390-3042del
NR_132124.1:n.154-3180del (TH2LCRR)
NM_005732.4:c.3390-3042del (RAD50) MANE Select	NP_005723.2:n.3390-3042del