Canonical Allele Identifier: CA1583246346

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604969T= , CM000667.2:g.132604969T=	GRCh38
NC_000005.9:g.131940661T= , CM000667.1:g.131940661T=	GRCh37
NC_000005.8:g.131968560T=	NCBI36
NG_021151.1:g.53046T=
NG_021151.2:g.52993T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2688T= MANE Select	ENSP00000368100.4:p.Thr896=
ENST00000638452.2:c.2391T=	ENSP00000492349.2:p.Thr797=
ENST00000638504.1:n.2296T=
ENST00000638568.2:c.2391T=	ENSP00000491158.2:p.Thr797=
ENST00000639899.1:n.3207T=
ENST00000640655.2:c.2391T=	ENSP00000491596.2:p.Thr797=
ENST00000651160.1:c.*832T=	ENSP00000498829.1:n.*832T=
ENST00000651723.1:c.*2771T=	ENSP00000498237.1:n.*2771T=
ENST00000652016.1:c.*905T=	ENSP00000498267.1:n.*905T=
ENST00000378823.7:c.2688T=	ENSP00000368100.4:p.Thr896=
ENST00000423956.5:c.*874T=	ENSP00000390971.1:n.*874T=
ENST00000533482.5:c.*2314T=	ENSP00000431225.1:n.*2314T=
NM_005732.3:c.2688T=	NP_005723.2:p.Thr896=
NM_005732.4:c.2688T= MANE Select	NP_005723.2:p.Thr896=