Canonical Allele Identifier: CA1583225285

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132575926A= , CM000667.2:g.132575926A=	GRCh38
NC_000005.9:g.131911618A= , CM000667.1:g.131911618A=	GRCh37
NC_000005.8:g.131939517A=	NCBI36
NG_021151.1:g.24003A=
NG_021151.2:g.23950A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.363A= MANE Select	ENSP00000368100.4:p.Thr121=
ENST00000638452.2:c.66A=	ENSP00000492349.2:p.Thr22=
ENST00000638504.1:n.440A=
ENST00000638568.2:c.66A=	ENSP00000491158.2:p.Thr22=
ENST00000639899.1:n.523A=
ENST00000640655.2:c.66A=	ENSP00000491596.2:p.Thr22=
ENST00000651160.1:c.363A=	ENSP00000498829.1:p.Thr121=
ENST00000651541.1:c.66A=	ENSP00000498795.1:p.Thr22=
ENST00000651658.1:n.431A=
ENST00000651723.1:c.*448+63A=	ENSP00000498237.1:n.*448+63A=
ENST00000652016.1:c.363A=	ENSP00000498267.1:p.Thr121=
ENST00000652485.1:c.363A=	ENSP00000498973.1:p.Thr121=
ENST00000378823.7:c.363A=	ENSP00000368100.4:p.Thr121=
ENST00000416135.5:c.66A=	ENSP00000389515.1:p.Thr22=
ENST00000423956.5:c.363A=	ENSP00000390971.1:p.Thr121=
ENST00000453394.5:c.363A=	ENSP00000400049.1:p.Thr121=
ENST00000533482.5:c.300+63A=	ENSP00000431225.1:n.300+63A=
NM_005732.3:c.363A=	NP_005723.2:p.Thr121=
NM_005732.4:c.363A= MANE Select	NP_005723.2:p.Thr121=