Canonical Allele Identifier: CA1583233508
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618080A= , CM000667.2:g.132618080A= GRCh38
NC_000005.9:g.131953772A= , CM000667.1:g.131953772A= GRCh37
NC_000005.8:g.131981671A= NCBI36
NG_021151.1:g.66157A=
NG_021151.2:g.66104A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3175A= MANE Select ENSP00000368100.4:p.Lys1059=
ENST00000638452.2:c.2878A= ENSP00000492349.2:p.Lys960=
ENST00000638504.1:n.2783A=
ENST00000638568.2:c.2878A= ENSP00000491158.2:p.Lys960=
ENST00000639899.1:n.3694A=
ENST00000640655.2:c.2878A= ENSP00000491596.2:p.Lys960=
ENST00000651249.1:c.11A=
ENST00000378823.7:c.3175A= ENSP00000368100.4:p.Lys1059=
ENST00000533482.5:c.*2801A= ENSP00000431225.1:n.*2801A=
NM_005732.3:c.3175A= NP_005723.2:p.Lys1059=
NM_005732.4:c.3175A= MANE Select NP_005723.2:p.Lys1059=