Canonical Allele Identifier: CA1583233452
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618042C= , CM000667.2:g.132618042C= GRCh38
NC_000005.9:g.131953734C= , CM000667.1:g.131953734C= GRCh37
NC_000005.8:g.131981633C= NCBI36
NG_021151.1:g.66119C=
NG_021151.2:g.66066C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3165-28C= MANE Select ENSP00000368100.4:n.3165-28C=
ENST00000638452.2:c.2868-28C= ENSP00000492349.2:n.2868-28C=
ENST00000638504.1:n.2773-28C=
ENST00000638568.2:c.2868-28C= ENSP00000491158.2:n.2868-28C=
ENST00000639899.1:n.3684-28C=
ENST00000640655.2:c.2868-28C= ENSP00000491596.2:n.2868-28C=
ENST00000378823.7:c.3165-28C= ENSP00000368100.4:n.3165-28C=
ENST00000533482.5:c.*2791-28C= ENSP00000431225.1:n.*2791-28C=
NM_005732.3:c.3165-28C= NP_005723.2:n.3165-28C=
NM_005732.4:c.3165-28C= MANE Select NP_005723.2:n.3165-28C=