Canonical Allele Identifier: CA1583254584
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132642211C= , CM000667.2:g.132642211C= GRCh38
NC_000005.9:g.131977903C= , CM000667.1:g.131977903C= GRCh37
NC_000005.8:g.132005802C= NCBI36
NG_021151.1:g.90288C=
NG_021151.2:g.90235C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3786C= (RAD50) MANE Select ENSP00000368100.4:p.Phe1262=
ENST00000638452.2:c.3489C= ENSP00000492349.2:p.Phe1163=
ENST00000638504.1:n.3394C=
ENST00000638568.2:c.3489C= ENSP00000491158.2:p.Phe1163=
ENST00000639899.1:n.4305C=
ENST00000640655.2:c.3489C= ENSP00000491596.2:p.Phe1163=
ENST00000651249.1:c.622C= (RAD50)
ENST00000378823.7:c.3786C= (RAD50) ENSP00000368100.4:p.Phe1262=
ENST00000455677.1:c.388-794C= (RAD50)
ENST00000533482.5:c.*3412C= (RAD50) ENSP00000431225.1:n.*3412C=
NM_005732.3:c.3786C= (RAD50) NP_005723.2:p.Phe1262=
NR_132125.1:n.176G= (TH2LCRR)
NR_132126.1:n.175-3946G= (TH2LCRR)
NM_005732.4:c.3786C= (RAD50) MANE Select NP_005723.2:p.Phe1262=