Canonical Allele Identifier: CA1583251587

Gene: RAD50 TH2LCRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132635271_132635275delinsAATTG , CM000667.2:g.132635271_132635275delinsAATTG	GRCh38
NC_000005.9:g.131970963_131970967delinsAATTG , CM000667.1:g.131970963_131970967delinsAATTG	GRCh37
NC_000005.8:g.131998862_131998866delinsAATTG	NCBI36
NG_021151.1:g.83348_83352delinsAATTG
NG_021151.2:g.83295_83299delinsAATTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3390-1844_3390-1840delinsAATTG (RAD50) MANE Select	ENSP00000368100.4:n.3390-1844_3390-1840delinsAATTG
ENST00000638452.2:c.3093-1844_3093-1840delinsAATTG	ENSP00000492349.2:n.3093-1844_3093-1840delinsAATTG
ENST00000638504.1:n.2998-1844_2998-1840delinsAATTG
ENST00000638568.2:c.3093-1844_3093-1840delinsAATTG	ENSP00000491158.2:n.3093-1844_3093-1840delinsAATTG
ENST00000639899.1:n.3909-1844_3909-1840delinsAATTG
ENST00000640655.2:c.3093-1844_3093-1840delinsAATTG	ENSP00000491596.2:n.3093-1844_3093-1840delinsAATTG
ENST00000651249.1:c.226-1844_226-1840delinsAATTG (RAD50)
ENST00000378823.7:c.3390-1844_3390-1840delinsAATTG (RAD50)	ENSP00000368100.4:n.3390-1844_3390-1840delinsAATTG
ENST00000455677.1:c.25-1844_25-1840delinsAATTG (RAD50)
ENST00000533482.5:c.*3016-1844_*3016-1840delinsAATTG (RAD50)	ENSP00000431225.1:n.*3016-1844_*3016-1840delinsAATTG
NM_005732.3:c.3390-1844_3390-1840delinsAATTG (RAD50)	NP_005723.2:n.3390-1844_3390-1840delinsAATTG
NR_132124.1:n.153+2883_153+2887delinsCAATT (TH2LCRR)
NM_005732.4:c.3390-1844_3390-1840delinsAATTG (RAD50) MANE Select	NP_005723.2:n.3390-1844_3390-1840delinsAATTG