Canonical Allele Identifier: CA1583241871

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595023G= , CM000667.2:g.132595023G=	GRCh38
NC_000005.9:g.131930715G= , CM000667.1:g.131930715G=	GRCh37
NC_000005.8:g.131958614G=	NCBI36
NG_021151.1:g.43100G=
NG_021151.2:g.43047G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1948G= MANE Select	ENSP00000368100.4:p.Glu650=
ENST00000638452.2:c.1651G=	ENSP00000492349.2:p.Glu551=
ENST00000638504.1:n.1480-81G=
ENST00000638568.2:c.1651G=	ENSP00000491158.2:p.Glu551=
ENST00000639899.1:n.2467G=
ENST00000640655.2:c.1651G=	ENSP00000491596.2:p.Glu551=
ENST00000651160.1:c.*16-81G=	ENSP00000498829.1:n.*16-81G=
ENST00000651658.1:n.2491G=
ENST00000651723.1:c.*2031G=	ENSP00000498237.1:n.*2031G=
ENST00000652016.1:c.*89-81G=	ENSP00000498267.1:n.*89-81G=
ENST00000652485.1:c.1981G=	ENSP00000498973.1:p.Glu661=
ENST00000378823.7:c.1948G=	ENSP00000368100.4:p.Glu650=
ENST00000423956.5:c.*134G=	ENSP00000390971.1:n.*134G=
ENST00000453394.5:c.1765G=	ENSP00000400049.1:p.Glu589=
ENST00000533482.5:c.*1574G=	ENSP00000431225.1:n.*1574G=
NM_005732.3:c.1948G=	NP_005723.2:p.Glu650=
NM_005732.4:c.1948G= MANE Select	NP_005723.2:p.Glu650=