Canonical Allele Identifier: CA1583216671
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556917A= , CM000667.2:g.132556917A= GRCh38
NC_000005.9:g.131892609A= , CM000667.1:g.131892609A= GRCh37
NC_000005.8:g.131920508A= NCBI36
NG_021151.1:g.4994A=
NG_021151.2:g.4941A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2367A= ENSP00000492349.2:n.-168-2367A=
ENST00000638504.1:n.207-2367A=
ENST00000638568.2:c.-169+444A= ENSP00000491158.2:n.-169+444A=
ENST00000639899.1:n.290-2367A=
ENST00000640655.2:c.-168-2367A= ENSP00000491596.2:n.-168-2367A=
ENST00000416135.5:c.-169+444A= ENSP00000389515.1:n.-169+444A=