Canonical Allele Identifier: CA1583216798

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557101C= , CM000667.2:g.132557101C=	GRCh38
NC_000005.9:g.131892793C= , CM000667.1:g.131892793C=	GRCh37
NC_000005.8:g.131920692C=	NCBI36
NG_021151.1:g.5178C=
NG_021151.2:g.5125C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.-224C= MANE Select	ENSP00000368100.4:n.-224C=
ENST00000638452.2:c.-168-2183C=	ENSP00000492349.2:n.-168-2183C=
ENST00000638504.1:n.207-2183C=
ENST00000638568.2:c.-169+628C=	ENSP00000491158.2:n.-169+628C=
ENST00000639899.1:n.290-2183C=
ENST00000640655.2:c.-168-2183C=	ENSP00000491596.2:n.-168-2183C=
ENST00000651160.1:c.-224C=	ENSP00000498829.1:n.-224C=
ENST00000651541.1:c.-169+92C=	ENSP00000498795.1:n.-169+92C=
ENST00000652016.1:c.-224C=	ENSP00000498267.1:n.-224C=
ENST00000652485.1:c.-224C=	ENSP00000498973.1:n.-224C=
ENST00000378823.7:c.-224C=	ENSP00000368100.4:n.-224C=
ENST00000416135.5:c.-169+628C=	ENSP00000389515.1:n.-169+628C=
ENST00000533482.5:c.-224C=	ENSP00000431225.1:n.-224C=
NM_005732.3:c.-224C=	NP_005723.2:n.-224C=
NM_005732.4:c.-224C= MANE Select	NP_005723.2:n.-224C=