Canonical Allele Identifier: CA1583229552

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609139T= , CM000667.2:g.132609139T=	GRCh38
NC_000005.9:g.131944831T= , CM000667.1:g.131944831T=	GRCh37
NC_000005.8:g.131972730T=	NCBI36
NG_021151.1:g.57216T=
NG_021151.2:g.57163T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2852T= MANE Select	ENSP00000368100.4:p.Val951=
ENST00000638452.2:c.2555T=	ENSP00000492349.2:p.Val852=
ENST00000638504.1:n.2460T=
ENST00000638568.2:c.2555T=	ENSP00000491158.2:p.Val852=
ENST00000639899.1:n.3371T=
ENST00000640655.2:c.2555T=	ENSP00000491596.2:p.Val852=
ENST00000651160.1:c.*996T=	ENSP00000498829.1:n.*996T=
ENST00000651723.1:c.*2935T=	ENSP00000498237.1:n.*2935T=
ENST00000378823.7:c.2852T=	ENSP00000368100.4:p.Val951=
ENST00000423956.5:c.*1038T=	ENSP00000390971.1:n.*1038T=
ENST00000533482.5:c.*2478T=	ENSP00000431225.1:n.*2478T=
NM_005732.3:c.2852T=	NP_005723.2:p.Val951=
NM_005732.4:c.2852T= MANE Select	NP_005723.2:p.Val951=