Canonical Allele Identifier: CA1583216889
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132557247C= , CM000667.2:g.132557247C= GRCh38
NC_000005.9:g.131892939C= , CM000667.1:g.131892939C= GRCh37
NC_000005.8:g.131920838C= NCBI36
NG_021151.1:g.5324C=
NG_021151.2:g.5271C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.-78C= MANE Select ENSP00000368100.4:n.-78C=
ENST00000638452.2:c.-168-2037C= ENSP00000492349.2:n.-168-2037C=
ENST00000638504.1:n.207-2037C=
ENST00000638568.2:c.-169+774C= ENSP00000491158.2:n.-169+774C=
ENST00000639899.1:n.290-2037C=
ENST00000640655.2:c.-168-2037C= ENSP00000491596.2:n.-168-2037C=
ENST00000651160.1:c.-78C= ENSP00000498829.1:n.-78C=
ENST00000651541.1:c.-169+238C= ENSP00000498795.1:n.-169+238C=
ENST00000651723.1:c.-78C= ENSP00000498237.1:n.-78C=
ENST00000652016.1:c.-78C= ENSP00000498267.1:n.-78C=
ENST00000652485.1:c.-78C= ENSP00000498973.1:n.-78C=
ENST00000378823.7:c.-78C= ENSP00000368100.4:n.-78C=
ENST00000416135.5:c.-169+774C= ENSP00000389515.1:n.-169+774C=
ENST00000423956.5:c.-78C= ENSP00000390971.1:n.-78C=
ENST00000453394.5:c.-78C= ENSP00000400049.1:n.-78C=
ENST00000533482.5:c.-78C= ENSP00000431225.1:n.-78C=
NM_005732.3:c.-78C= NP_005723.2:n.-78C=
NM_005732.4:c.-78C= MANE Select NP_005723.2:n.-78C=