Canonical Allele Identifier: CA1583241855

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594986T= , CM000667.2:g.132594986T=	GRCh38
NC_000005.9:g.131930678T= , CM000667.1:g.131930678T=	GRCh37
NC_000005.8:g.131958577T=	NCBI36
NG_021151.1:g.43063T=
NG_021151.2:g.43010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1911T= MANE Select	ENSP00000368100.4:p.Asp637=
ENST00000638452.2:c.1614T=	ENSP00000492349.2:p.Asp538=
ENST00000638504.1:n.1480-118T=
ENST00000638568.2:c.1614T=	ENSP00000491158.2:p.Asp538=
ENST00000639899.1:n.2430T=
ENST00000640655.2:c.1614T=	ENSP00000491596.2:p.Asp538=
ENST00000651160.1:c.*16-118T=	ENSP00000498829.1:n.*16-118T=
ENST00000651658.1:n.2454T=
ENST00000651723.1:c.*1994T=	ENSP00000498237.1:n.*1994T=
ENST00000652016.1:c.*89-118T=	ENSP00000498267.1:n.*89-118T=
ENST00000652485.1:c.1944T=	ENSP00000498973.1:p.Asp648=
ENST00000378823.7:c.1911T=	ENSP00000368100.4:p.Asp637=
ENST00000423956.5:c.*97T=	ENSP00000390971.1:n.*97T=
ENST00000453394.5:c.1728T=	ENSP00000400049.1:p.Asp576=
ENST00000533482.5:c.*1537T=	ENSP00000431225.1:n.*1537T=
NM_005732.3:c.1911T=	NP_005723.2:p.Asp637=
NM_005732.4:c.1911T= MANE Select	NP_005723.2:p.Asp637=