Canonical Allele Identifier: CA1583254559
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132642173T= , CM000667.2:g.132642173T= GRCh38
NC_000005.9:g.131977865T= , CM000667.1:g.131977865T= GRCh37
NC_000005.8:g.132005764T= NCBI36
NG_021151.1:g.90250T=
NG_021151.2:g.90197T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3753-5T= (RAD50) MANE Select ENSP00000368100.4:n.3753-5T=
ENST00000638452.2:c.3456-5T= ENSP00000492349.2:n.3456-5T=
ENST00000638504.1:n.3361-5T=
ENST00000638568.2:c.3456-5T= ENSP00000491158.2:n.3456-5T=
ENST00000639899.1:n.4272-5T=
ENST00000640655.2:c.3456-5T= ENSP00000491596.2:n.3456-5T=
ENST00000651249.1:c.589-5T= (RAD50)
ENST00000378823.7:c.3753-5T= (RAD50) ENSP00000368100.4:n.3753-5T=
ENST00000455677.1:c.388-832T= (RAD50)
ENST00000533482.5:c.*3379-5T= (RAD50) ENSP00000431225.1:n.*3379-5T=
NM_005732.3:c.3753-5T= (RAD50) NP_005723.2:n.3753-5T=
NR_132125.1:n.189+25A= (TH2LCRR)
NR_132126.1:n.175-3908A= (TH2LCRR)
NM_005732.4:c.3753-5T= (RAD50) MANE Select NP_005723.2:n.3753-5T=