Canonical Allele Identifier: CA1583246235
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132604744_132604745delinsTG , CM000667.2:g.132604744_132604745delinsTG GRCh38
NC_000005.9:g.131940436_131940437delinsTG , CM000667.1:g.131940436_131940437delinsTG GRCh37
NC_000005.8:g.131968335_131968336delinsTG NCBI36
NG_021151.1:g.52821_52822delinsTG
NG_021151.2:g.52768_52769delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.2525-62_2525-61delinsTG MANE Select ENSP00000368100.4:n.2525-62_2525-61delinsTG
ENST00000638452.2:c.2228-62_2228-61delinsTG ENSP00000492349.2:n.2228-62_2228-61delinsTG
ENST00000638504.1:n.2133-62_2133-61delinsTG
ENST00000638568.2:c.2228-62_2228-61delinsTG ENSP00000491158.2:n.2228-62_2228-61delinsTG
ENST00000639899.1:n.3044-62_3044-61delinsTG
ENST00000640655.2:c.2228-62_2228-61delinsTG ENSP00000491596.2:n.2228-62_2228-61delinsTG
ENST00000651160.1:c.*669-62_*669-61delinsTG ENSP00000498829.1:n.*669-62_*669-61delinsTG
ENST00000651723.1:c.*2608-62_*2608-61delinsTG ENSP00000498237.1:n.*2608-62_*2608-61delinsTG
ENST00000652016.1:c.*742-62_*742-61delinsTG ENSP00000498267.1:n.*742-62_*742-61delinsTG
ENST00000652485.1:c.2558-62_2558-61delinsTG ENSP00000498973.1:n.2558-62_2558-61delinsTG
ENST00000378823.7:c.2525-62_2525-61delinsTG ENSP00000368100.4:n.2525-62_2525-61delinsTG
ENST00000423956.5:c.*711-62_*711-61delinsTG ENSP00000390971.1:n.*711-62_*711-61delinsTG
ENST00000533482.5:c.*2151-62_*2151-61delinsTG ENSP00000431225.1:n.*2151-62_*2151-61delinsTG
NM_005732.3:c.2525-62_2525-61delinsTG NP_005723.2:n.2525-62_2525-61delinsTG
NM_005732.4:c.2525-62_2525-61delinsTG MANE Select NP_005723.2:n.2525-62_2525-61delinsTG