Canonical Allele Identifier: CA1583229563

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609154G= , CM000667.2:g.132609154G=	GRCh38
NC_000005.9:g.131944846G= , CM000667.1:g.131944846G=	GRCh37
NC_000005.8:g.131972745G=	NCBI36
NG_021151.1:g.57231G=
NG_021151.2:g.57178G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2867G= MANE Select	ENSP00000368100.4:p.Gly956=
ENST00000638452.2:c.2570G=	ENSP00000492349.2:p.Gly857=
ENST00000638504.1:n.2475G=
ENST00000638568.2:c.2570G=	ENSP00000491158.2:p.Gly857=
ENST00000639899.1:n.3386G=
ENST00000640655.2:c.2570G=	ENSP00000491596.2:p.Gly857=
ENST00000651160.1:c.*1011G=	ENSP00000498829.1:n.*1011G=
ENST00000651723.1:c.*2950G=	ENSP00000498237.1:n.*2950G=
ENST00000378823.7:c.2867G=	ENSP00000368100.4:p.Gly956=
ENST00000423956.5:c.*1053G=	ENSP00000390971.1:n.*1053G=
ENST00000533482.5:c.*2493G=	ENSP00000431225.1:n.*2493G=
NM_005732.3:c.2867G=	NP_005723.2:p.Gly956=
NM_005732.4:c.2867G= MANE Select	NP_005723.2:p.Gly956=