Canonical Allele Identifier: CA2675217935
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132604993_132604996del , CM000667.2:g.132604993_132604996del GRCh38
NC_000005.9:g.131940685_131940688del , CM000667.1:g.131940685_131940688del GRCh37
NC_000005.8:g.131968584_131968587del NCBI36
NG_021151.1:g.53070_53073del
NG_021151.2:g.53017_53020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.2712_2715del MANE Select ENSP00000368100.4:p.Ile905ArgfsTer7
ENST00000638452.2:c.2415_2418del ENSP00000492349.2:p.Ile806ArgfsTer7
ENST00000638504.1:n.2320_2323del
ENST00000638568.2:c.2415_2418del ENSP00000491158.2:p.Ile806ArgfsTer7
ENST00000639899.1:n.3231_3234del
ENST00000640655.2:c.2415_2418del ENSP00000491596.2:p.Ile806ArgfsTer7
ENST00000651160.1:c.*856_*859del ENSP00000498829.1:n.*856_*859del
ENST00000651723.1:c.*2795_*2798del ENSP00000498237.1:n.*2795_*2798del
ENST00000652016.1:c.*929_*932del ENSP00000498267.1:n.*929_*932del
ENST00000378823.7:c.2712_2715del ENSP00000368100.4:p.Ile905ArgfsTer7
ENST00000423956.5:c.*898_*901del ENSP00000390971.1:n.*898_*901del
ENST00000533482.5:c.*2338_*2341del ENSP00000431225.1:n.*2338_*2341del
NM_005732.3:c.2712_2715del NP_005723.2:p.Ile905ArgfsTer7
NM_005732.4:c.2712_2715del MANE Select NP_005723.2:p.Ile905ArgfsTer7