Canonical Allele Identifier: CA1583229562

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609153G= , CM000667.2:g.132609153G=	GRCh38
NC_000005.9:g.131944845G= , CM000667.1:g.131944845G=	GRCh37
NC_000005.8:g.131972744G=	NCBI36
NG_021151.1:g.57230G=
NG_021151.2:g.57177G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2866G= MANE Select	ENSP00000368100.4:p.Gly956=
ENST00000638452.2:c.2569G=	ENSP00000492349.2:p.Gly857=
ENST00000638504.1:n.2474G=
ENST00000638568.2:c.2569G=	ENSP00000491158.2:p.Gly857=
ENST00000639899.1:n.3385G=
ENST00000640655.2:c.2569G=	ENSP00000491596.2:p.Gly857=
ENST00000651160.1:c.*1010G=	ENSP00000498829.1:n.*1010G=
ENST00000651723.1:c.*2949G=	ENSP00000498237.1:n.*2949G=
ENST00000378823.7:c.2866G=	ENSP00000368100.4:p.Gly956=
ENST00000423956.5:c.*1052G=	ENSP00000390971.1:n.*1052G=
ENST00000533482.5:c.*2492G=	ENSP00000431225.1:n.*2492G=
NM_005732.3:c.2866G=	NP_005723.2:p.Gly956=
NM_005732.4:c.2866G= MANE Select	NP_005723.2:p.Gly956=