Canonical Allele Identifier: CA1583241864

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595007G= , CM000667.2:g.132595007G=	GRCh38
NC_000005.9:g.131930699G= , CM000667.1:g.131930699G=	GRCh37
NC_000005.8:g.131958598G=	NCBI36
NG_021151.1:g.43084G=
NG_021151.2:g.43031G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1932G= MANE Select	ENSP00000368100.4:p.Arg644=
ENST00000638452.2:c.1635G=	ENSP00000492349.2:p.Arg545=
ENST00000638504.1:n.1480-97G=
ENST00000638568.2:c.1635G=	ENSP00000491158.2:p.Arg545=
ENST00000639899.1:n.2451G=
ENST00000640655.2:c.1635G=	ENSP00000491596.2:p.Arg545=
ENST00000651160.1:c.*16-97G=	ENSP00000498829.1:n.*16-97G=
ENST00000651658.1:n.2475G=
ENST00000651723.1:c.*2015G=	ENSP00000498237.1:n.*2015G=
ENST00000652016.1:c.*89-97G=	ENSP00000498267.1:n.*89-97G=
ENST00000652485.1:c.1965G=	ENSP00000498973.1:p.Arg655=
ENST00000378823.7:c.1932G=	ENSP00000368100.4:p.Arg644=
ENST00000423956.5:c.*118G=	ENSP00000390971.1:n.*118G=
ENST00000453394.5:c.1749G=	ENSP00000400049.1:p.Arg583=
ENST00000533482.5:c.*1558G=	ENSP00000431225.1:n.*1558G=
NM_005732.3:c.1932G=	NP_005723.2:p.Arg644=
NM_005732.4:c.1932G= MANE Select	NP_005723.2:p.Arg644=