Canonical Allele Identifier: CA2510105497

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618511_132618512insA , CM000667.2:g.132618511_132618512insA	GRCh38
NC_000005.9:g.131954203_131954204insA , CM000667.1:g.131954203_131954204insA	GRCh37
NC_000005.8:g.131982102_131982103insA	NCBI36
NG_021151.1:g.66588_66589insA
NG_021151.2:g.66535_66536insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3389+217_3389+218insA MANE Select	ENSP00000368100.4:n.3389+217_3389+218insA
ENST00000638452.2:c.3092+217_3092+218insA	ENSP00000492349.2:n.3092+217_3092+218insA
ENST00000638504.1:n.2997+217_2997+218insA
ENST00000638568.2:c.3092+217_3092+218insA	ENSP00000491158.2:n.3092+217_3092+218insA
ENST00000639899.1:n.3908+217_3908+218insA
ENST00000640655.2:c.3092+217_3092+218insA	ENSP00000491596.2:n.3092+217_3092+218insA
ENST00000651249.1:c.225+217_225+218insA
ENST00000378823.7:c.3389+217_3389+218insA	ENSP00000368100.4:n.3389+217_3389+218insA
ENST00000455677.1:c.24+217_24+218insA
ENST00000533482.5:c.*3015+217_*3015+218insA	ENSP00000431225.1:n.*3015+217_*3015+218insA
NM_005732.3:c.3389+217_3389+218insA	NP_005723.2:n.3389+217_3389+218insA
NM_005732.4:c.3389+217_3389+218insA MANE Select	NP_005723.2:n.3389+217_3389+218insA