Canonical Allele Identifier: CA1583251132
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132634223T= , CM000667.2:g.132634223T= GRCh38
NC_000005.9:g.131969915T= , CM000667.1:g.131969915T= GRCh37
NC_000005.8:g.131997814T= NCBI36
NG_021151.1:g.82300T=
NG_021151.2:g.82247T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.3390-2892T= (RAD50) MANE Select ENSP00000368100.4:n.3390-2892T=
ENST00000638452.2:c.3093-2892T= ENSP00000492349.2:n.3093-2892T=
ENST00000638504.1:n.2998-2892T=
ENST00000638568.2:c.3093-2892T= ENSP00000491158.2:n.3093-2892T=
ENST00000639899.1:n.3909-2892T=
ENST00000640655.2:c.3093-2892T= ENSP00000491596.2:n.3093-2892T=
ENST00000651249.1:c.226-2892T= (RAD50)
ENST00000378823.7:c.3390-2892T= (RAD50) ENSP00000368100.4:n.3390-2892T=
ENST00000455677.1:c.25-2892T= (RAD50)
ENST00000533482.5:c.*3016-2892T= (RAD50) ENSP00000431225.1:n.*3016-2892T=
NM_005732.3:c.3390-2892T= (RAD50) NP_005723.2:n.3390-2892T=
NR_132124.1:n.154-3332A= (TH2LCRR)
NM_005732.4:c.3390-2892T= (RAD50) MANE Select NP_005723.2:n.3390-2892T=