Canonical Allele Identifier: CA1583226860

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579352C= , CM000667.2:g.132579352C=	GRCh38
NC_000005.9:g.131915044C= , CM000667.1:g.131915044C=	GRCh37
NC_000005.8:g.131942943C=	NCBI36
NG_021151.1:g.27429C=
NG_021151.2:g.27376C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.401C= MANE Select	ENSP00000368100.4:p.Ala134=
ENST00000638452.2:c.104C=	ENSP00000492349.2:p.Ala35=
ENST00000638504.1:n.442+3424C=
ENST00000638568.2:c.104C=	ENSP00000491158.2:p.Ala35=
ENST00000639899.1:n.561C=
ENST00000640655.2:c.104C=	ENSP00000491596.2:p.Ala35=
ENST00000651160.1:c.401C=	ENSP00000498829.1:p.Ala134=
ENST00000651541.1:c.104C=	ENSP00000498795.1:p.Ala35=
ENST00000651658.1:n.469C=
ENST00000651723.1:c.*484C=	ENSP00000498237.1:n.*484C=
ENST00000652016.1:c.401C=	ENSP00000498267.1:p.Ala134=
ENST00000652485.1:c.401C=	ENSP00000498973.1:p.Ala134=
ENST00000378823.7:c.401C=	ENSP00000368100.4:p.Ala134=
ENST00000416135.5:c.104C=	ENSP00000389515.1:p.Ala35=
ENST00000423956.5:c.401C=	ENSP00000390971.1:p.Ala134=
ENST00000453394.5:c.401C=	ENSP00000400049.1:p.Ala134=
ENST00000533482.5:c.*27C=	ENSP00000431225.1:n.*27C=
NM_005732.3:c.401C=	NP_005723.2:p.Ala134=
NM_005732.4:c.401C= MANE Select	NP_005723.2:p.Ala134=