Canonical Allele Identifier: CA1583241829

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594942T= , CM000667.2:g.132594942T=	GRCh38
NC_000005.9:g.131930634T= , CM000667.1:g.131930634T=	GRCh37
NC_000005.8:g.131958533T=	NCBI36
NG_021151.1:g.43019T=
NG_021151.2:g.42966T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1867T= MANE Select	ENSP00000368100.4:p.Ser623=
ENST00000638452.2:c.1570T=	ENSP00000492349.2:p.Ser524=
ENST00000638504.1:n.1480-162T=
ENST00000638568.2:c.1570T=	ENSP00000491158.2:p.Ser524=
ENST00000639899.1:n.2386T=
ENST00000640655.2:c.1570T=	ENSP00000491596.2:p.Ser524=
ENST00000651160.1:c.*16-162T=	ENSP00000498829.1:n.*16-162T=
ENST00000651658.1:n.2410T=
ENST00000651723.1:c.*1950T=	ENSP00000498237.1:n.*1950T=
ENST00000652016.1:c.*89-162T=	ENSP00000498267.1:n.*89-162T=
ENST00000652485.1:c.1900T=	ENSP00000498973.1:p.Ser634=
ENST00000378823.7:c.1867T=	ENSP00000368100.4:p.Ser623=
ENST00000423956.5:c.*53T=	ENSP00000390971.1:n.*53T=
ENST00000453394.5:c.1684T=	ENSP00000400049.1:p.Ser562=
ENST00000533482.5:c.*1493T=	ENSP00000431225.1:n.*1493T=
NM_005732.3:c.1867T=	NP_005723.2:p.Ser623=
NM_005732.4:c.1867T= MANE Select	NP_005723.2:p.Ser623=