Canonical Allele Identifier: CA1583251558

Gene: RAD50 TH2LCRR

Linked Data

• dbSNP Id: rs1751556884

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132635227_132635228del , CM000667.2:g.132635227_132635228del	GRCh38
NC_000005.9:g.131970919_131970920del , CM000667.1:g.131970919_131970920del	GRCh37
NC_000005.8:g.131998818_131998819del	NCBI36
NG_021151.1:g.83304_83305del
NG_021151.2:g.83251_83252del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3390-1888_3390-1887del (RAD50) MANE Select	ENSP00000368100.4:n.3390-1888_3390-1887de...
ENST00000638452.2:c.3093-1888_3093-1887del	ENSP00000492349.2:n.3093-1888_3093-1887de...
ENST00000638504.1:n.2998-1888_2998-1887del
ENST00000638568.2:c.3093-1888_3093-1887del	ENSP00000491158.2:n.3093-1888_3093-1887de...
ENST00000639899.1:n.3909-1888_3909-1887del
ENST00000640655.2:c.3093-1888_3093-1887del	ENSP00000491596.2:n.3093-1888_3093-1887de...
ENST00000651249.1:c.226-1888_226-1887del (RAD50)
ENST00000378823.7:c.3390-1888_3390-1887del (RAD50)	ENSP00000368100.4:n.3390-1888_3390-1887de...
ENST00000455677.1:c.25-1888_25-1887del (RAD50)
ENST00000533482.5:c.*3016-1888_*3016-1887del (RAD50)	ENSP00000431225.1:n.*3016-1888_*3016-1887...
NM_005732.3:c.3390-1888_3390-1887del (RAD50)	NP_005723.2:n.3390-1888_3390-1887del
NR_132124.1:n.153+2933_153+2934del (TH2LCRR)
NM_005732.4:c.3390-1888_3390-1887del (RAD50) MANE Select	NP_005723.2:n.3390-1888_3390-1887del