Canonical Allele Identifier: CA1583233623
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618107A= , CM000667.2:g.132618107A= GRCh38
NC_000005.9:g.131953799A= , CM000667.1:g.131953799A= GRCh37
NC_000005.8:g.131981698A= NCBI36
NG_021151.1:g.66184A=
NG_021151.2:g.66131A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3202A= MANE Select ENSP00000368100.4:p.Lys1068=
ENST00000638452.2:c.2905A= ENSP00000492349.2:p.Lys969=
ENST00000638504.1:n.2810A=
ENST00000638568.2:c.2905A= ENSP00000491158.2:p.Lys969=
ENST00000639899.1:n.3721A=
ENST00000640655.2:c.2905A= ENSP00000491596.2:p.Lys969=
ENST00000651249.1:c.38A=
ENST00000378823.7:c.3202A= ENSP00000368100.4:p.Lys1068=
ENST00000533482.5:c.*2828A= ENSP00000431225.1:n.*2828A=
NM_005732.3:c.3202A= NP_005723.2:p.Lys1068=
NM_005732.4:c.3202A= MANE Select NP_005723.2:p.Lys1068=