Canonical Allele Identifier: CA1583239507

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589800A= , CM000667.2:g.132589800A=	GRCh38
NC_000005.9:g.131925492A= , CM000667.1:g.131925492A=	GRCh37
NC_000005.8:g.131953391A=	NCBI36
NG_021151.1:g.37877A=
NG_021151.2:g.37824A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1415A= MANE Select	ENSP00000368100.4:p.Asp472=
ENST00000638452.2:c.1118A=	ENSP00000492349.2:p.Asp373=
ENST00000638504.1:n.1101A=
ENST00000638568.2:c.1118A=	ENSP00000491158.2:p.Asp373=
ENST00000639899.1:n.1934A=
ENST00000640655.2:c.1118A=	ENSP00000491596.2:p.Asp373=
ENST00000651160.1:c.1415A=	ENSP00000498829.1:p.Asp472=
ENST00000651541.1:c.1118A=	ENSP00000498795.1:p.Asp373=
ENST00000651658.1:n.1842A=
ENST00000651723.1:c.*1498A=	ENSP00000498237.1:n.*1498A=
ENST00000652016.1:c.1415A=	ENSP00000498267.1:p.Asp472=
ENST00000652485.1:c.1415A=	ENSP00000498973.1:p.Asp472=
ENST00000378823.7:c.1415A=	ENSP00000368100.4:p.Asp472=
ENST00000423956.5:c.1415A=	ENSP00000390971.1:p.Asp472=
ENST00000453394.5:c.1415A=	ENSP00000400049.1:p.Asp472=
ENST00000533482.5:c.*1041A=	ENSP00000431225.1:n.*1041A=
NM_005732.3:c.1415A=	NP_005723.2:p.Asp472=
NM_005732.4:c.1415A= MANE Select	NP_005723.2:p.Asp472=