Canonical Allele Identifier: CA1583237999
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132588686G= , CM000667.2:g.132588686G= GRCh38
NC_000005.9:g.131924378G= , CM000667.1:g.131924378G= GRCh37
NC_000005.8:g.131952277G= NCBI36
NG_021151.1:g.36763G=
NG_021151.2:g.36710G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.1052-1G= MANE Select ENSP00000368100.4:n.1052-1G=
ENST00000638452.2:c.755-1G= ENSP00000492349.2:n.755-1G=
ENST00000638504.1:n.738-1G=
ENST00000638568.2:c.755-1G= ENSP00000491158.2:n.755-1G=
ENST00000639899.1:n.1571-1G=
ENST00000640655.2:c.755-1G= ENSP00000491596.2:n.755-1G=
ENST00000651160.1:c.1052-1G= ENSP00000498829.1:n.1052-1G=
ENST00000651541.1:c.755-1G= ENSP00000498795.1:n.755-1G=
ENST00000651658.1:n.1479-1G=
ENST00000651723.1:c.*1135-1G= ENSP00000498237.1:n.*1135-1G=
ENST00000652016.1:c.1052-1G= ENSP00000498267.1:n.1052-1G=
ENST00000652485.1:c.1052-1G= ENSP00000498973.1:n.1052-1G=
ENST00000378823.7:c.1052-1G= ENSP00000368100.4:n.1052-1G=
ENST00000423956.5:c.1052-1G= ENSP00000390971.1:n.1052-1G=
ENST00000453394.5:c.1052-1G= ENSP00000400049.1:n.1052-1G=
ENST00000487596.1:n.618-1G=
ENST00000533482.5:c.*678-1G= ENSP00000431225.1:n.*678-1G=
NM_005732.3:c.1052-1G= NP_005723.2:n.1052-1G=
NM_005732.4:c.1052-1G= MANE Select NP_005723.2:n.1052-1G=