Canonical Allele Identifier: CA1583234142

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618438G= , CM000667.2:g.132618438G=	GRCh38
NC_000005.9:g.131954130G= , CM000667.1:g.131954130G=	GRCh37
NC_000005.8:g.131982029G=	NCBI36
NG_021151.1:g.66515G=
NG_021151.2:g.66462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3389+144G= MANE Select	ENSP00000368100.4:n.3389+144G=
ENST00000638452.2:c.3092+144G=	ENSP00000492349.2:n.3092+144G=
ENST00000638504.1:n.2997+144G=
ENST00000638568.2:c.3092+144G=	ENSP00000491158.2:n.3092+144G=
ENST00000639899.1:n.3908+144G=
ENST00000640655.2:c.3092+144G=	ENSP00000491596.2:n.3092+144G=
ENST00000651249.1:c.225+144G=
ENST00000378823.7:c.3389+144G=	ENSP00000368100.4:n.3389+144G=
ENST00000455677.1:c.24+144G=
ENST00000533482.5:c.*3015+144G=	ENSP00000431225.1:n.*3015+144G=
NM_005732.3:c.3389+144G=	NP_005723.2:n.3389+144G=
NM_005732.4:c.3389+144G= MANE Select	NP_005723.2:n.3389+144G=