Canonical Allele Identifier: CA1583239681

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589874_132589877delinsTATA , CM000667.2:g.132589874_132589877delinsTATA	GRCh38
NC_000005.9:g.131925566_131925569delinsTATA , CM000667.1:g.131925566_131925569delinsTATA	GRCh37
NC_000005.8:g.131953465_131953468delinsTATA	NCBI36
NG_021151.1:g.37951_37954delinsTATA
NG_021151.2:g.37898_37901delinsTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1452+37_1452+40delinsTATA MANE Select	ENSP00000368100.4:n.1452+37_1452+40delinsTATA
ENST00000638452.2:c.1155+37_1155+40delinsTATA	ENSP00000492349.2:n.1155+37_1155+40delinsTATA
ENST00000638504.1:n.1138+37_1138+40delinsTATA
ENST00000638568.2:c.1155+37_1155+40delinsTATA	ENSP00000491158.2:n.1155+37_1155+40delinsTATA
ENST00000639899.1:n.1971+37_1971+40delinsTATA
ENST00000640655.2:c.1155+37_1155+40delinsTATA	ENSP00000491596.2:n.1155+37_1155+40delinsTATA
ENST00000651160.1:c.1452+37_1452+40delinsTATA	ENSP00000498829.1:n.1452+37_1452+40delinsTATA
ENST00000651541.1:c.1155+37_1155+40delinsTATA	ENSP00000498795.1:n.1155+37_1155+40delinsTATA
ENST00000651658.1:n.1879+37_1879+40delinsTATA
ENST00000651723.1:c.*1535+37_*1535+40delinsTATA	ENSP00000498237.1:n.*1535+37_*1535+40delinsTATA
ENST00000652016.1:c.1452+37_1452+40delinsTATA	ENSP00000498267.1:n.1452+37_1452+40delinsTATA
ENST00000652485.1:c.1452+37_1452+40delinsTATA	ENSP00000498973.1:n.1452+37_1452+40delinsTATA
ENST00000378823.7:c.1452+37_1452+40delinsTATA	ENSP00000368100.4:n.1452+37_1452+40delinsTATA
ENST00000423956.5:c.1452+37_1452+40delinsTATA	ENSP00000390971.1:n.1452+37_1452+40delinsTATA
ENST00000453394.5:c.1452+37_1452+40delinsTATA	ENSP00000400049.1:n.1452+37_1452+40delinsTATA
ENST00000533482.5:c.*1078+37_*1078+40delinsTATA	ENSP00000431225.1:n.*1078+37_*1078+40delinsTATA
NM_005732.3:c.1452+37_1452+40delinsTATA	NP_005723.2:n.1452+37_1452+40delinsTATA
NM_005732.4:c.1452+37_1452+40delinsTATA MANE Select	NP_005723.2:n.1452+37_1452+40delinsTATA