Canonical Allele Identifier: CA1583225253

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132575865T= , CM000667.2:g.132575865T=	GRCh38
NC_000005.9:g.131911557T= , CM000667.1:g.131911557T=	GRCh37
NC_000005.8:g.131939456T=	NCBI36
NG_021151.1:g.23942T=
NG_021151.2:g.23889T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.302T= MANE Select	ENSP00000368100.4:p.Val101=
ENST00000638452.2:c.5T=	ENSP00000492349.2:p.Val2=
ENST00000638504.1:n.379T=
ENST00000638568.2:c.5T=	ENSP00000491158.2:p.Val2=
ENST00000639899.1:n.462T=
ENST00000640655.2:c.5T=	ENSP00000491596.2:p.Val2=
ENST00000651160.1:c.302T=	ENSP00000498829.1:p.Val101=
ENST00000651541.1:c.5T=	ENSP00000498795.1:p.Val2=
ENST00000651658.1:n.370T=
ENST00000651723.1:c.*448+2T=	ENSP00000498237.1:n.*448+2T=
ENST00000652016.1:c.302T=	ENSP00000498267.1:p.Val101=
ENST00000652485.1:c.302T=	ENSP00000498973.1:p.Val101=
ENST00000378823.7:c.302T=	ENSP00000368100.4:p.Val101=
ENST00000416135.5:c.5T=	ENSP00000389515.1:p.Val2=
ENST00000423956.5:c.302T=	ENSP00000390971.1:p.Val101=
ENST00000453394.5:c.302T=	ENSP00000400049.1:p.Val101=
ENST00000533482.5:c.300+2T=	ENSP00000431225.1:n.300+2T=
NM_005732.3:c.302T=	NP_005723.2:p.Val101=
NM_005732.4:c.302T= MANE Select	NP_005723.2:p.Val101=