Canonical Allele Identifier: CA1583246254

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604786G= , CM000667.2:g.132604786G=	GRCh38
NC_000005.9:g.131940478G= , CM000667.1:g.131940478G=	GRCh37
NC_000005.8:g.131968377G=	NCBI36
NG_021151.1:g.52863G=
NG_021151.2:g.52810G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2525-20G= MANE Select	ENSP00000368100.4:n.2525-20G=
ENST00000638452.2:c.2228-20G=	ENSP00000492349.2:n.2228-20G=
ENST00000638504.1:n.2133-20G=
ENST00000638568.2:c.2228-20G=	ENSP00000491158.2:n.2228-20G=
ENST00000639899.1:n.3044-20G=
ENST00000640655.2:c.2228-20G=	ENSP00000491596.2:n.2228-20G=
ENST00000651160.1:c.*669-20G=	ENSP00000498829.1:n.*669-20G=
ENST00000651723.1:c.*2608-20G=	ENSP00000498237.1:n.*2608-20G=
ENST00000652016.1:c.*742-20G=	ENSP00000498267.1:n.*742-20G=
ENST00000652485.1:c.2558-20G=	ENSP00000498973.1:n.2558-20G=
ENST00000378823.7:c.2525-20G=	ENSP00000368100.4:n.2525-20G=
ENST00000423956.5:c.*711-20G=	ENSP00000390971.1:n.*711-20G=
ENST00000533482.5:c.*2151-20G=	ENSP00000431225.1:n.*2151-20G=
NM_005732.3:c.2525-20G=	NP_005723.2:n.2525-20G=
NM_005732.4:c.2525-20G= MANE Select	NP_005723.2:n.2525-20G=