Canonical Allele Identifier: CA1583229589

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609202A= , CM000667.2:g.132609202A=	GRCh38
NC_000005.9:g.131944894A= , CM000667.1:g.131944894A=	GRCh37
NC_000005.8:g.131972793A=	NCBI36
NG_021151.1:g.57279A=
NG_021151.2:g.57226A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2915A= MANE Select	ENSP00000368100.4:p.Tyr972=
ENST00000638452.2:c.2618A=	ENSP00000492349.2:p.Tyr873=
ENST00000638504.1:n.2523A=
ENST00000638568.2:c.2618A=	ENSP00000491158.2:p.Tyr873=
ENST00000639899.1:n.3434A=
ENST00000640655.2:c.2618A=	ENSP00000491596.2:p.Tyr873=
ENST00000651160.1:c.*1059A=	ENSP00000498829.1:n.*1059A=
ENST00000651723.1:c.*2998A=	ENSP00000498237.1:n.*2998A=
ENST00000378823.7:c.2915A=	ENSP00000368100.4:p.Tyr972=
ENST00000423956.5:c.*1101A=	ENSP00000390971.1:n.*1101A=
ENST00000533482.5:c.*2541A=	ENSP00000431225.1:n.*2541A=
NM_005732.3:c.2915A=	NP_005723.2:p.Tyr972=
NM_005732.4:c.2915A= MANE Select	NP_005723.2:p.Tyr972=