Canonical Allele Identifier: CA1583234084

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618366_132618367delinsAT , CM000667.2:g.132618366_132618367delinsAT	GRCh38
NC_000005.9:g.131954058_131954059delinsAT , CM000667.1:g.131954058_131954059delinsAT	GRCh37
NC_000005.8:g.131981957_131981958delinsAT	NCBI36
NG_021151.1:g.66443_66444delinsAT
NG_021151.2:g.66390_66391delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3389+72_3389+73delinsAT MANE Select	ENSP00000368100.4:n.3389+72_3389+73delinsAT
ENST00000638452.2:c.3092+72_3092+73delinsAT	ENSP00000492349.2:n.3092+72_3092+73delinsAT
ENST00000638504.1:n.2997+72_2997+73delinsAT
ENST00000638568.2:c.3092+72_3092+73delinsAT	ENSP00000491158.2:n.3092+72_3092+73delinsAT
ENST00000639899.1:n.3908+72_3908+73delinsAT
ENST00000640655.2:c.3092+72_3092+73delinsAT	ENSP00000491596.2:n.3092+72_3092+73delinsAT
ENST00000651249.1:c.225+72_225+73delinsAT
ENST00000378823.7:c.3389+72_3389+73delinsAT	ENSP00000368100.4:n.3389+72_3389+73delinsAT
ENST00000455677.1:c.24+72_24+73delinsAT
ENST00000533482.5:c.*3015+72_*3015+73delinsAT	ENSP00000431225.1:n.*3015+72_*3015+73delinsAT
NM_005732.3:c.3389+72_3389+73delinsAT	NP_005723.2:n.3389+72_3389+73delinsAT
NM_005732.4:c.3389+72_3389+73delinsAT MANE Select	NP_005723.2:n.3389+72_3389+73delinsAT