Canonical Allele Identifier: CA1583216697
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556963G= , CM000667.2:g.132556963G= GRCh38
NC_000005.9:g.131892655G= , CM000667.1:g.131892655G= GRCh37
NC_000005.8:g.131920554G= NCBI36
NG_021151.1:g.5040G=
NG_021151.2:g.4987G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2321G= ENSP00000492349.2:n.-168-2321G=
ENST00000638504.1:n.207-2321G=
ENST00000638568.2:c.-169+490G= ENSP00000491158.2:n.-169+490G=
ENST00000639899.1:n.290-2321G=
ENST00000640655.2:c.-168-2321G= ENSP00000491596.2:n.-168-2321G=
ENST00000651541.1:c.-215G= ENSP00000498795.1:n.-215G=
ENST00000378823.7:c.-362G= ENSP00000368100.4:n.-362G=
ENST00000416135.5:c.-169+490G= ENSP00000389515.1:n.-169+490G=
ENST00000533482.5:c.-362G= ENSP00000431225.1:n.-362G=
NM_005732.3:c.-362G= NP_005723.2:n.-362G=