Canonical Allele Identifier: CA1583245900
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132604021A= , CM000667.2:g.132604021A= GRCh38
NC_000005.9:g.131939713A= , CM000667.1:g.131939713A= GRCh37
NC_000005.8:g.131967612A= NCBI36
NG_021151.1:g.52098A=
NG_021151.2:g.52045A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.2499A= MANE Select ENSP00000368100.4:p.Gln833=
ENST00000638452.2:c.2202A= ENSP00000492349.2:p.Gln734=
ENST00000638504.1:n.2107A=
ENST00000638568.2:c.2202A= ENSP00000491158.2:p.Gln734=
ENST00000639899.1:n.3018A=
ENST00000640655.2:c.2202A= ENSP00000491596.2:p.Gln734=
ENST00000651160.1:c.*643A= ENSP00000498829.1:n.*643A=
ENST00000651658.1:n.3042A=
ENST00000651723.1:c.*2582A= ENSP00000498237.1:n.*2582A=
ENST00000652016.1:c.*716A= ENSP00000498267.1:n.*716A=
ENST00000652485.1:c.2532A= ENSP00000498973.1:p.Gln844=
ENST00000378823.7:c.2499A= ENSP00000368100.4:p.Gln833=
ENST00000423956.5:c.*685A= ENSP00000390971.1:n.*685A=
ENST00000533482.5:c.*2125A= ENSP00000431225.1:n.*2125A=
NM_005732.3:c.2499A= NP_005723.2:p.Gln833=
NM_005732.4:c.2499A= MANE Select NP_005723.2:p.Gln833=