Canonical Allele Identifier: CA1583233457
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618046_132618048delinsATT , CM000667.2:g.132618046_132618048delinsATT GRCh38
NC_000005.9:g.131953738_131953740delinsATT , CM000667.1:g.131953738_131953740delinsATT GRCh37
NC_000005.8:g.131981637_131981639delinsATT NCBI36
NG_021151.1:g.66123_66125delinsATT
NG_021151.2:g.66070_66072delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3165-24_3165-22delinsATT MANE Select ENSP00000368100.4:n.3165-24_3165-22delinsATT
ENST00000638452.2:c.2868-24_2868-22delinsATT ENSP00000492349.2:n.2868-24_2868-22delinsATT
ENST00000638504.1:n.2773-24_2773-22delinsATT
ENST00000638568.2:c.2868-24_2868-22delinsATT ENSP00000491158.2:n.2868-24_2868-22delinsATT
ENST00000639899.1:n.3684-24_3684-22delinsATT
ENST00000640655.2:c.2868-24_2868-22delinsATT ENSP00000491596.2:n.2868-24_2868-22delinsATT
ENST00000378823.7:c.3165-24_3165-22delinsATT ENSP00000368100.4:n.3165-24_3165-22delinsATT
ENST00000533482.5:c.*2791-24_*2791-22delinsATT ENSP00000431225.1:n.*2791-24_*2791-22delinsATT
NM_005732.3:c.3165-24_3165-22delinsATT NP_005723.2:n.3165-24_3165-22delinsATT
NM_005732.4:c.3165-24_3165-22delinsATT MANE Select NP_005723.2:n.3165-24_3165-22delinsATT