Canonical Allele Identifier: CA1583229560
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132609151A= , CM000667.2:g.132609151A= GRCh38
NC_000005.9:g.131944843A= , CM000667.1:g.131944843A= GRCh37
NC_000005.8:g.131972742A= NCBI36
NG_021151.1:g.57228A=
NG_021151.2:g.57175A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.2864A= MANE Select ENSP00000368100.4:p.His955=
ENST00000638452.2:c.2567A= ENSP00000492349.2:p.His856=
ENST00000638504.1:n.2472A=
ENST00000638568.2:c.2567A= ENSP00000491158.2:p.His856=
ENST00000639899.1:n.3383A=
ENST00000640655.2:c.2567A= ENSP00000491596.2:p.His856=
ENST00000651160.1:c.*1008A= ENSP00000498829.1:n.*1008A=
ENST00000651723.1:c.*2947A= ENSP00000498237.1:n.*2947A=
ENST00000378823.7:c.2864A= ENSP00000368100.4:p.His955=
ENST00000423956.5:c.*1050A= ENSP00000390971.1:n.*1050A=
ENST00000533482.5:c.*2490A= ENSP00000431225.1:n.*2490A=
NM_005732.3:c.2864A= NP_005723.2:p.His955=
NM_005732.4:c.2864A= MANE Select NP_005723.2:p.His955=