Canonical Allele Identifier: CA1583251055
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132634035_132634036delinsAT , CM000667.2:g.132634035_132634036delinsAT GRCh38
NC_000005.9:g.131969727_131969728delinsAT , CM000667.1:g.131969727_131969728delinsAT GRCh37
NC_000005.8:g.131997626_131997627delinsAT NCBI36
NG_021151.1:g.82112_82113delinsAT
NG_021151.2:g.82059_82060delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3390-3080_3390-3079delinsAT (RAD50) MANE Select ENSP00000368100.4:n.3390-3080_3390-3079delinsAT
ENST00000638452.2:c.3093-3080_3093-3079delinsAT ENSP00000492349.2:n.3093-3080_3093-3079delinsAT
ENST00000638504.1:n.2998-3080_2998-3079delinsAT
ENST00000638568.2:c.3093-3080_3093-3079delinsAT ENSP00000491158.2:n.3093-3080_3093-3079delinsAT
ENST00000639899.1:n.3909-3080_3909-3079delinsAT
ENST00000640655.2:c.3093-3080_3093-3079delinsAT ENSP00000491596.2:n.3093-3080_3093-3079delinsAT
ENST00000651249.1:c.226-3080_226-3079delinsAT (RAD50)
ENST00000378823.7:c.3390-3080_3390-3079delinsAT (RAD50) ENSP00000368100.4:n.3390-3080_3390-3079delinsAT
ENST00000455677.1:c.25-3080_25-3079delinsAT (RAD50)
ENST00000533482.5:c.*3016-3080_*3016-3079delinsAT (RAD50) ENSP00000431225.1:n.*3016-3080_*3016-3079delinsAT
NM_005732.3:c.3390-3080_3390-3079delinsAT (RAD50) NP_005723.2:n.3390-3080_3390-3079delinsAT
NR_132124.1:n.154-3145_154-3144delinsAT (TH2LCRR)
NM_005732.4:c.3390-3080_3390-3079delinsAT (RAD50) MANE Select NP_005723.2:n.3390-3080_3390-3079delinsAT