Canonical Allele Identifier: CA1583216764

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557038T= , CM000667.2:g.132557038T=	GRCh38
NC_000005.9:g.131892730T= , CM000667.1:g.131892730T=	GRCh37
NC_000005.8:g.131920629T=	NCBI36
NG_021151.1:g.5115T=
NG_021151.2:g.5062T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.-287T= MANE Select	ENSP00000368100.4:n.-287T=
ENST00000638452.2:c.-168-2246T=	ENSP00000492349.2:n.-168-2246T=
ENST00000638504.1:n.207-2246T=
ENST00000638568.2:c.-169+565T=	ENSP00000491158.2:n.-169+565T=
ENST00000639899.1:n.290-2246T=
ENST00000640655.2:c.-168-2246T=	ENSP00000491596.2:n.-168-2246T=
ENST00000651160.1:c.-287T=	ENSP00000498829.1:n.-287T=
ENST00000651541.1:c.-169+29T=	ENSP00000498795.1:n.-169+29T=
ENST00000652016.1:c.-287T=	ENSP00000498267.1:n.-287T=
ENST00000652485.1:c.-287T=	ENSP00000498973.1:n.-287T=
ENST00000378823.7:c.-287T=	ENSP00000368100.4:n.-287T=
ENST00000416135.5:c.-169+565T=	ENSP00000389515.1:n.-169+565T=
ENST00000533482.5:c.-287T=	ENSP00000431225.1:n.-287T=
NM_005732.3:c.-287T=	NP_005723.2:n.-287T=
NM_005732.4:c.-287T= MANE Select	NP_005723.2:n.-287T=