Canonical Allele Identifier: CA1583254696
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132642398G= , CM000667.2:g.132642398G= GRCh38
NC_000005.9:g.131978090G= , CM000667.1:g.131978090G= GRCh37
NC_000005.8:g.132005989G= NCBI36
NG_021151.1:g.90475G=
NG_021151.2:g.90422G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.*34G= (RAD50) MANE Select ENSP00000368100.4:n.*34G=
ENST00000638452.2:c.*34G= ENSP00000492349.2:n.*34G=
ENST00000638504.1:n.3581G=
ENST00000638568.2:c.*34G= ENSP00000491158.2:n.*34G=
ENST00000639899.1:n.4492G=
ENST00000640655.2:c.*34G= ENSP00000491596.2:n.*34G=
ENST00000651249.1:c.805+4G= (RAD50)
ENST00000378823.7:c.*34G= (RAD50) ENSP00000368100.4:n.*34G=
ENST00000455677.1:c.388-607G= (RAD50)
ENST00000533482.5:c.*3599G= (RAD50) ENSP00000431225.1:n.*3599G=
NM_005732.3:c.*34G= (RAD50) NP_005723.2:n.*34G=
NR_132125.1:n.105-116C= (TH2LCRR)
NR_132126.1:n.175-4133C= (TH2LCRR)
NM_005732.4:c.*34G= (RAD50) MANE Select NP_005723.2:n.*34G=