Canonical Allele Identifier: CA1583241803

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594899A= , CM000667.2:g.132594899A=	GRCh38
NC_000005.9:g.131930591A= , CM000667.1:g.131930591A=	GRCh37
NC_000005.8:g.131958490A=	NCBI36
NG_021151.1:g.42976A=
NG_021151.2:g.42923A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1824A= MANE Select	ENSP00000368100.4:p.Lys608=
ENST00000638452.2:c.1527A=	ENSP00000492349.2:p.Lys509=
ENST00000638504.1:n.1480-205A=
ENST00000638568.2:c.1527A=	ENSP00000491158.2:p.Lys509=
ENST00000639899.1:n.2343A=
ENST00000640655.2:c.1527A=	ENSP00000491596.2:p.Lys509=
ENST00000651160.1:c.*16-205A=	ENSP00000498829.1:n.*16-205A=
ENST00000651658.1:n.2367A=
ENST00000651723.1:c.*1907A=	ENSP00000498237.1:n.*1907A=
ENST00000652016.1:c.*89-205A=	ENSP00000498267.1:n.*89-205A=
ENST00000652485.1:c.1857A=	ENSP00000498973.1:p.Lys619=
ENST00000378823.7:c.1824A=	ENSP00000368100.4:p.Lys608=
ENST00000423956.5:c.*10A=	ENSP00000390971.1:n.*10A=
ENST00000453394.5:c.1641A=	ENSP00000400049.1:p.Lys547=
ENST00000533482.5:c.*1450A=	ENSP00000431225.1:n.*1450A=
NM_005732.3:c.1824A=	NP_005723.2:p.Lys608=
NM_005732.4:c.1824A= MANE Select	NP_005723.2:p.Lys608=