Canonical Allele Identifier: CA1583241843

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594966G= , CM000667.2:g.132594966G=	GRCh38
NC_000005.9:g.131930658G= , CM000667.1:g.131930658G=	GRCh37
NC_000005.8:g.131958557G=	NCBI36
NG_021151.1:g.43043G=
NG_021151.2:g.42990G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1891G= MANE Select	ENSP00000368100.4:p.Asp631=
ENST00000638452.2:c.1594G=	ENSP00000492349.2:p.Asp532=
ENST00000638504.1:n.1480-138G=
ENST00000638568.2:c.1594G=	ENSP00000491158.2:p.Asp532=
ENST00000639899.1:n.2410G=
ENST00000640655.2:c.1594G=	ENSP00000491596.2:p.Asp532=
ENST00000651160.1:c.*16-138G=	ENSP00000498829.1:n.*16-138G=
ENST00000651658.1:n.2434G=
ENST00000651723.1:c.*1974G=	ENSP00000498237.1:n.*1974G=
ENST00000652016.1:c.*89-138G=	ENSP00000498267.1:n.*89-138G=
ENST00000652485.1:c.1924G=	ENSP00000498973.1:p.Asp642=
ENST00000378823.7:c.1891G=	ENSP00000368100.4:p.Asp631=
ENST00000423956.5:c.*77G=	ENSP00000390971.1:n.*77G=
ENST00000453394.5:c.1708G=	ENSP00000400049.1:p.Asp570=
ENST00000533482.5:c.*1517G=	ENSP00000431225.1:n.*1517G=
NM_005732.3:c.1891G=	NP_005723.2:p.Asp631=
NM_005732.4:c.1891G= MANE Select	NP_005723.2:p.Asp631=