Canonical Allele Identifier: CA1583216774

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557059G= , CM000667.2:g.132557059G=	GRCh38
NC_000005.9:g.131892751G= , CM000667.1:g.131892751G=	GRCh37
NC_000005.8:g.131920650G=	NCBI36
NG_021151.1:g.5136G=
NG_021151.2:g.5083G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.-266G= MANE Select	ENSP00000368100.4:n.-266G=
ENST00000638452.2:c.-168-2225G=	ENSP00000492349.2:n.-168-2225G=
ENST00000638504.1:n.207-2225G=
ENST00000638568.2:c.-169+586G=	ENSP00000491158.2:n.-169+586G=
ENST00000639899.1:n.290-2225G=
ENST00000640655.2:c.-168-2225G=	ENSP00000491596.2:n.-168-2225G=
ENST00000651160.1:c.-266G=	ENSP00000498829.1:n.-266G=
ENST00000651541.1:c.-169+50G=	ENSP00000498795.1:n.-169+50G=
ENST00000652016.1:c.-266G=	ENSP00000498267.1:n.-266G=
ENST00000652485.1:c.-266G=	ENSP00000498973.1:n.-266G=
ENST00000378823.7:c.-266G=	ENSP00000368100.4:n.-266G=
ENST00000416135.5:c.-169+586G=	ENSP00000389515.1:n.-169+586G=
ENST00000533482.5:c.-266G=	ENSP00000431225.1:n.-266G=
NM_005732.3:c.-266G=	NP_005723.2:n.-266G=
NM_005732.4:c.-266G= MANE Select	NP_005723.2:n.-266G=