Canonical Allele Identifier: CA1583241858

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594997A= , CM000667.2:g.132594997A=	GRCh38
NC_000005.9:g.131930689A= , CM000667.1:g.131930689A=	GRCh37
NC_000005.8:g.131958588A=	NCBI36
NG_021151.1:g.43074A=
NG_021151.2:g.43021A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1922A= MANE Select	ENSP00000368100.4:p.Asp641=
ENST00000638452.2:c.1625A=	ENSP00000492349.2:p.Asp542=
ENST00000638504.1:n.1480-107A=
ENST00000638568.2:c.1625A=	ENSP00000491158.2:p.Asp542=
ENST00000639899.1:n.2441A=
ENST00000640655.2:c.1625A=	ENSP00000491596.2:p.Asp542=
ENST00000651160.1:c.*16-107A=	ENSP00000498829.1:n.*16-107A=
ENST00000651658.1:n.2465A=
ENST00000651723.1:c.*2005A=	ENSP00000498237.1:n.*2005A=
ENST00000652016.1:c.*89-107A=	ENSP00000498267.1:n.*89-107A=
ENST00000652485.1:c.1955A=	ENSP00000498973.1:p.Asp652=
ENST00000378823.7:c.1922A=	ENSP00000368100.4:p.Asp641=
ENST00000423956.5:c.*108A=	ENSP00000390971.1:n.*108A=
ENST00000453394.5:c.1739A=	ENSP00000400049.1:p.Asp580=
ENST00000533482.5:c.*1548A=	ENSP00000431225.1:n.*1548A=
NM_005732.3:c.1922A=	NP_005723.2:p.Asp641=
NM_005732.4:c.1922A= MANE Select	NP_005723.2:p.Asp641=