Canonical Allele Identifier: CA1583216689
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556952T= , CM000667.2:g.132556952T= GRCh38
NC_000005.9:g.131892644T= , CM000667.1:g.131892644T= GRCh37
NC_000005.8:g.131920543T= NCBI36
NG_021151.1:g.5029T=
NG_021151.2:g.4976T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2332T= ENSP00000492349.2:n.-168-2332T=
ENST00000638504.1:n.207-2332T=
ENST00000638568.2:c.-169+479T= ENSP00000491158.2:n.-169+479T=
ENST00000639899.1:n.290-2332T=
ENST00000640655.2:c.-168-2332T= ENSP00000491596.2:n.-168-2332T=
ENST00000651541.1:c.-226T= ENSP00000498795.1:n.-226T=
ENST00000378823.7:c.-373T= ENSP00000368100.4:n.-373T=
ENST00000416135.5:c.-169+479T= ENSP00000389515.1:n.-169+479T=
ENST00000533482.5:c.-373T= ENSP00000431225.1:n.-373T=
NM_005732.3:c.-373T= NP_005723.2:n.-373T=