Canonical Allele Identifier: CA1583241836

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594953A= , CM000667.2:g.132594953A=	GRCh38
NC_000005.9:g.131930645A= , CM000667.1:g.131930645A=	GRCh37
NC_000005.8:g.131958544A=	NCBI36
NG_021151.1:g.43030A=
NG_021151.2:g.42977A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1878A= MANE Select	ENSP00000368100.4:p.Glu626=
ENST00000638452.2:c.1581A=	ENSP00000492349.2:p.Glu527=
ENST00000638504.1:n.1480-151A=
ENST00000638568.2:c.1581A=	ENSP00000491158.2:p.Glu527=
ENST00000639899.1:n.2397A=
ENST00000640655.2:c.1581A=	ENSP00000491596.2:p.Glu527=
ENST00000651160.1:c.*16-151A=	ENSP00000498829.1:n.*16-151A=
ENST00000651658.1:n.2421A=
ENST00000651723.1:c.*1961A=	ENSP00000498237.1:n.*1961A=
ENST00000652016.1:c.*89-151A=	ENSP00000498267.1:n.*89-151A=
ENST00000652485.1:c.1911A=	ENSP00000498973.1:p.Glu637=
ENST00000378823.7:c.1878A=	ENSP00000368100.4:p.Glu626=
ENST00000423956.5:c.*64A=	ENSP00000390971.1:n.*64A=
ENST00000453394.5:c.1695A=	ENSP00000400049.1:p.Glu565=
ENST00000533482.5:c.*1504A=	ENSP00000431225.1:n.*1504A=
NM_005732.3:c.1878A=	NP_005723.2:p.Glu626=
NM_005732.4:c.1878A= MANE Select	NP_005723.2:p.Glu626=