Canonical Allele Identifier: CA1583252484
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132637510_132637527delinsCTCTTTTTTTTTTCTTTT , CM000667.2:g.132637510_132637527delinsCTCTTTTTTTTTTCTTTT GRCh38
NC_000005.9:g.131973202_131973219delinsCTCTTTTTTTTTTCTTTT , CM000667.1:g.131973202_131973219delinsCTCTTTTTTTTTTCTTTT GRCh37
NC_000005.8:g.132001101_132001118delinsCTCTTTTTTTTTTCTTTT NCBI36
NG_021151.1:g.85587_85604delinsCTCTTTTTTTTTTCTTTT
NG_021151.2:g.85534_85551delinsCTCTTTTTTTTTTCTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT (RAD50) MANE Select ENSP00000368100.4:n.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT...
ENST00000638452.2:c.3178+310_3178+327delinsCTCTTTTTTTTTTCTTTT ENSP00000492349.2:n.3178+310_3178+327delinsCTCTTTTTTTTTTCTTTT...
ENST00000638504.1:n.3083+310_3083+327delinsCTCTTTTTTTTTTCTTTT
ENST00000638568.2:c.3178+310_3178+327delinsCTCTTTTTTTTTTCTTTT ENSP00000491158.2:n.3178+310_3178+327delinsCTCTTTTTTTTTTCTTTT...
ENST00000639899.1:n.3994+310_3994+327delinsCTCTTTTTTTTTTCTTTT
ENST00000640655.2:c.3178+310_3178+327delinsCTCTTTTTTTTTTCTTTT ENSP00000491596.2:n.3178+310_3178+327delinsCTCTTTTTTTTTTCTTTT...
ENST00000651249.1:c.311+310_311+327delinsCTCTTTTTTTTTTCTTTT (RAD50)
ENST00000378823.7:c.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT (RAD50) ENSP00000368100.4:n.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT...
ENST00000455677.1:c.110+310_110+327delinsCTCTTTTTTTTTTCTTTT (RAD50)
ENST00000533482.5:c.*3101+310_*3101+327delinsCTCTTTTTTTTTTCTTTT (RAD50) ENSP00000431225.1:n.*3101+310_*3101+327delinsCTCTTTTTTTTTTCTT...
NM_005732.3:c.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT (RAD50) NP_005723.2:n.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT
NR_132124.1:n.153+631_153+648delinsAAAAGAAAAAAAAAAGAG (TH2LCRR)
NM_005732.4:c.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT (RAD50) MANE Select NP_005723.2:n.3475+310_3475+327delinsCTCTTTTTTTTTTCTTTT