Canonical Allele Identifier: CA1583246243

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604762C= , CM000667.2:g.132604762C=	GRCh38
NC_000005.9:g.131940454C= , CM000667.1:g.131940454C=	GRCh37
NC_000005.8:g.131968353C=	NCBI36
NG_021151.1:g.52839C=
NG_021151.2:g.52786C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2525-44C= MANE Select	ENSP00000368100.4:n.2525-44C=
ENST00000638452.2:c.2228-44C=	ENSP00000492349.2:n.2228-44C=
ENST00000638504.1:n.2133-44C=
ENST00000638568.2:c.2228-44C=	ENSP00000491158.2:n.2228-44C=
ENST00000639899.1:n.3044-44C=
ENST00000640655.2:c.2228-44C=	ENSP00000491596.2:n.2228-44C=
ENST00000651160.1:c.*669-44C=	ENSP00000498829.1:n.*669-44C=
ENST00000651723.1:c.*2608-44C=	ENSP00000498237.1:n.*2608-44C=
ENST00000652016.1:c.*742-44C=	ENSP00000498267.1:n.*742-44C=
ENST00000652485.1:c.2558-44C=	ENSP00000498973.1:n.2558-44C=
ENST00000378823.7:c.2525-44C=	ENSP00000368100.4:n.2525-44C=
ENST00000423956.5:c.*711-44C=	ENSP00000390971.1:n.*711-44C=
ENST00000533482.5:c.*2151-44C=	ENSP00000431225.1:n.*2151-44C=
NM_005732.3:c.2525-44C=	NP_005723.2:n.2525-44C=
NM_005732.4:c.2525-44C= MANE Select	NP_005723.2:n.2525-44C=