Canonical Allele Identifier: CA1583216684
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556940A= , CM000667.2:g.132556940A= GRCh38
NC_000005.9:g.131892632A= , CM000667.1:g.131892632A= GRCh37
NC_000005.8:g.131920531A= NCBI36
NG_021151.1:g.5017A=
NG_021151.2:g.4964A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2344A= ENSP00000492349.2:n.-168-2344A=
ENST00000638504.1:n.207-2344A=
ENST00000638568.2:c.-169+467A= ENSP00000491158.2:n.-169+467A=
ENST00000639899.1:n.290-2344A=
ENST00000640655.2:c.-168-2344A= ENSP00000491596.2:n.-168-2344A=
ENST00000651541.1:c.-238A= ENSP00000498795.1:n.-238A=
ENST00000378823.7:c.-385A= ENSP00000368100.4:n.-385A=
ENST00000416135.5:c.-169+467A= ENSP00000389515.1:n.-169+467A=
ENST00000533482.5:c.-385A= ENSP00000431225.1:n.-385A=
NM_005732.3:c.-385A= NP_005723.2:n.-385A=