Canonical Allele Identifier: CA1583240622

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591961A= , CM000667.2:g.132591961A=	GRCh38
NC_000005.9:g.131927653A= , CM000667.1:g.131927653A=	GRCh37
NC_000005.8:g.131955552A=	NCBI36
NG_021151.1:g.40038A=
NG_021151.2:g.39985A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1720A= MANE Select	ENSP00000368100.4:p.Lys574=
ENST00000638452.2:c.1423A=	ENSP00000492349.2:p.Lys475=
ENST00000638504.1:n.1406A=
ENST00000638568.2:c.1423A=	ENSP00000491158.2:p.Lys475=
ENST00000639899.1:n.2239A=
ENST00000640655.2:c.1423A=	ENSP00000491596.2:p.Lys475=
ENST00000651160.1:c.1720A=	ENSP00000498829.1:p.Lys574=
ENST00000651541.1:c.1423A=	ENSP00000498795.1:p.Lys475=
ENST00000651658.1:n.2147A=
ENST00000651723.1:c.*1803A=	ENSP00000498237.1:n.*1803A=
ENST00000652016.1:c.1720A=	ENSP00000498267.1:p.Lys574=
ENST00000652485.1:c.1753A=	ENSP00000498973.1:p.Lys585=
ENST00000378823.7:c.1720A=	ENSP00000368100.4:p.Lys574=
ENST00000423956.5:c.1635+555A=	ENSP00000390971.1:n.1635+555A=
ENST00000434288.1:c.215A=
ENST00000453394.5:c.1537A=	ENSP00000400049.1:p.Lys513=
ENST00000533482.5:c.*1346A=	ENSP00000431225.1:n.*1346A=
NM_005732.3:c.1720A=	NP_005723.2:p.Lys574=
NM_005732.4:c.1720A= MANE Select	NP_005723.2:p.Lys574=