Canonical Allele Identifier: CA1583233468
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618053_132618054delinsAT , CM000667.2:g.132618053_132618054delinsAT GRCh38
NC_000005.9:g.131953745_131953746delinsAT , CM000667.1:g.131953745_131953746delinsAT GRCh37
NC_000005.8:g.131981644_131981645delinsAT NCBI36
NG_021151.1:g.66130_66131delinsAT
NG_021151.2:g.66077_66078delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3165-17_3165-16delinsAT MANE Select ENSP00000368100.4:n.3165-17_3165-16delinsAT
ENST00000638452.2:c.2868-17_2868-16delinsAT ENSP00000492349.2:n.2868-17_2868-16delinsAT
ENST00000638504.1:n.2773-17_2773-16delinsAT
ENST00000638568.2:c.2868-17_2868-16delinsAT ENSP00000491158.2:n.2868-17_2868-16delinsAT
ENST00000639899.1:n.3684-17_3684-16delinsAT
ENST00000640655.2:c.2868-17_2868-16delinsAT ENSP00000491596.2:n.2868-17_2868-16delinsAT
ENST00000378823.7:c.3165-17_3165-16delinsAT ENSP00000368100.4:n.3165-17_3165-16delinsAT
ENST00000533482.5:c.*2791-17_*2791-16delinsAT ENSP00000431225.1:n.*2791-17_*2791-16delinsAT
NM_005732.3:c.3165-17_3165-16delinsAT NP_005723.2:n.3165-17_3165-16delinsAT
NM_005732.4:c.3165-17_3165-16delinsAT MANE Select NP_005723.2:n.3165-17_3165-16delinsAT