Canonical Allele Identifier: CA1583240613

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591943G= , CM000667.2:g.132591943G=	GRCh38
NC_000005.9:g.131927635G= , CM000667.1:g.131927635G=	GRCh37
NC_000005.8:g.131955534G=	NCBI36
NG_021151.1:g.40020G=
NG_021151.2:g.39967G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1702G= MANE Select	ENSP00000368100.4:p.Gly568=
ENST00000638452.2:c.1405G=	ENSP00000492349.2:p.Gly469=
ENST00000638504.1:n.1388G=
ENST00000638568.2:c.1405G=	ENSP00000491158.2:p.Gly469=
ENST00000639899.1:n.2221G=
ENST00000640655.2:c.1405G=	ENSP00000491596.2:p.Gly469=
ENST00000651160.1:c.1702G=	ENSP00000498829.1:p.Gly568=
ENST00000651541.1:c.1405G=	ENSP00000498795.1:p.Gly469=
ENST00000651658.1:n.2129G=
ENST00000651723.1:c.*1785G=	ENSP00000498237.1:n.*1785G=
ENST00000652016.1:c.1702G=	ENSP00000498267.1:p.Gly568=
ENST00000652485.1:c.1735G=	ENSP00000498973.1:p.Gly579=
ENST00000378823.7:c.1702G=	ENSP00000368100.4:p.Gly568=
ENST00000423956.5:c.1635+537G=	ENSP00000390971.1:n.1635+537G=
ENST00000434288.1:c.197G=
ENST00000453394.5:c.1519G=	ENSP00000400049.1:p.Gly507=
ENST00000533482.5:c.*1328G=	ENSP00000431225.1:n.*1328G=
NM_005732.3:c.1702G=	NP_005723.2:p.Gly568=
NM_005732.4:c.1702G= MANE Select	NP_005723.2:p.Gly568=