Canonical Allele Identifier: CA1583216695
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556960T= , CM000667.2:g.132556960T= GRCh38
NC_000005.9:g.131892652T= , CM000667.1:g.131892652T= GRCh37
NC_000005.8:g.131920551T= NCBI36
NG_021151.1:g.5037T=
NG_021151.2:g.4984T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2324T= ENSP00000492349.2:n.-168-2324T=
ENST00000638504.1:n.207-2324T=
ENST00000638568.2:c.-169+487T= ENSP00000491158.2:n.-169+487T=
ENST00000639899.1:n.290-2324T=
ENST00000640655.2:c.-168-2324T= ENSP00000491596.2:n.-168-2324T=
ENST00000651541.1:c.-218T= ENSP00000498795.1:n.-218T=
ENST00000378823.7:c.-365T= ENSP00000368100.4:n.-365T=
ENST00000416135.5:c.-169+487T= ENSP00000389515.1:n.-169+487T=
ENST00000533482.5:c.-365T= ENSP00000431225.1:n.-365T=
NM_005732.3:c.-365T= NP_005723.2:n.-365T=