Canonical Allele Identifier: CA2675215490
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556957G>T , CM000667.2:g.132556957G>T GRCh38
NC_000005.9:g.131892649G>T , CM000667.1:g.131892649G>T GRCh37
NC_000005.8:g.131920548G>T NCBI36
NG_021151.1:g.5034G>T
NG_021151.2:g.4981G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2327G>T ENSP00000492349.2:n.-168-2327G>T
ENST00000638504.1:n.207-2327G>T
ENST00000638568.2:c.-169+484G>T ENSP00000491158.2:n.-169+484G>T
ENST00000639899.1:n.290-2327G>T
ENST00000640655.2:c.-168-2327G>T ENSP00000491596.2:n.-168-2327G>T
ENST00000651541.1:c.-221G>T ENSP00000498795.1:n.-221G>T
ENST00000378823.7:c.-368G>T ENSP00000368100.4:n.-368G>T
ENST00000416135.5:c.-169+484G>T ENSP00000389515.1:n.-169+484G>T
ENST00000533482.5:c.-368G>T ENSP00000431225.1:n.-368G>T
NM_005732.3:c.-368G>T NP_005723.2:n.-368G>T