Canonical Allele Identifier: CA1583216677
Gene: RAD50 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556932C= , CM000667.2:g.132556932C= GRCh38
NC_000005.9:g.131892624C= , CM000667.1:g.131892624C= GRCh37
NC_000005.8:g.131920523C= NCBI36
NG_021151.1:g.5009C=
NG_021151.2:g.4956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2352C= ENSP00000492349.2:n.-168-2352C=
ENST00000638504.1:n.207-2352C=
ENST00000638568.2:c.-169+459C= ENSP00000491158.2:n.-169+459C=
ENST00000639899.1:n.290-2352C=
ENST00000640655.2:c.-168-2352C= ENSP00000491596.2:n.-168-2352C=
ENST00000651541.1:c.-246C= ENSP00000498795.1:n.-246C=
ENST00000416135.5:c.-169+459C= ENSP00000389515.1:n.-169+459C=
NM_005732.3:c.-393C= NP_005723.2:n.-393C=
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