Canonical Allele Identifier: CA1583246287
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132604859A= , CM000667.2:g.132604859A= GRCh38
NC_000005.9:g.131940551A= , CM000667.1:g.131940551A= GRCh37
NC_000005.8:g.131968450A= NCBI36
NG_021151.1:g.52936A=
NG_021151.2:g.52883A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.2578A= MANE Select ENSP00000368100.4:p.Ile860=
ENST00000638452.2:c.2281A= ENSP00000492349.2:p.Ile761=
ENST00000638504.1:n.2186A=
ENST00000638568.2:c.2281A= ENSP00000491158.2:p.Ile761=
ENST00000639899.1:n.3097A=
ENST00000640655.2:c.2281A= ENSP00000491596.2:p.Ile761=
ENST00000651160.1:c.*722A= ENSP00000498829.1:n.*722A=
ENST00000651723.1:c.*2661A= ENSP00000498237.1:n.*2661A=
ENST00000652016.1:c.*795A= ENSP00000498267.1:n.*795A=
ENST00000652485.1:c.2611A= ENSP00000498973.1:p.Ile871=
ENST00000378823.7:c.2578A= ENSP00000368100.4:p.Ile860=
ENST00000423956.5:c.*764A= ENSP00000390971.1:n.*764A=
ENST00000533482.5:c.*2204A= ENSP00000431225.1:n.*2204A=
NM_005732.3:c.2578A= NP_005723.2:p.Ile860=
NM_005732.4:c.2578A= MANE Select NP_005723.2:p.Ile860=