Canonical Allele Identifier: CA1583233689
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618127A= , CM000667.2:g.132618127A= GRCh38
NC_000005.9:g.131953819A= , CM000667.1:g.131953819A= GRCh37
NC_000005.8:g.131981718A= NCBI36
NG_021151.1:g.66204A=
NG_021151.2:g.66151A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3222A= MANE Select ENSP00000368100.4:p.Ala1074=
ENST00000638452.2:c.2925A= ENSP00000492349.2:p.Ala975=
ENST00000638504.1:n.2830A=
ENST00000638568.2:c.2925A= ENSP00000491158.2:p.Ala975=
ENST00000639899.1:n.3741A=
ENST00000640655.2:c.2925A= ENSP00000491596.2:p.Ala975=
ENST00000651249.1:c.58A=
ENST00000378823.7:c.3222A= ENSP00000368100.4:p.Ala1074=
ENST00000533482.5:c.*2848A= ENSP00000431225.1:n.*2848A=
NM_005732.3:c.3222A= NP_005723.2:p.Ala1074=
NM_005732.4:c.3222A= MANE Select NP_005723.2:p.Ala1074=