Canonical Allele Identifier: CA1583246271

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604813T= , CM000667.2:g.132604813T=	GRCh38
NC_000005.9:g.131940505T= , CM000667.1:g.131940505T=	GRCh37
NC_000005.8:g.131968404T=	NCBI36
NG_021151.1:g.52890T=
NG_021151.2:g.52837T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2532T= MANE Select	ENSP00000368100.4:p.Ser844=
ENST00000638452.2:c.2235T=	ENSP00000492349.2:p.Ser745=
ENST00000638504.1:n.2140T=
ENST00000638568.2:c.2235T=	ENSP00000491158.2:p.Ser745=
ENST00000639899.1:n.3051T=
ENST00000640655.2:c.2235T=	ENSP00000491596.2:p.Ser745=
ENST00000651160.1:c.*676T=	ENSP00000498829.1:n.*676T=
ENST00000651723.1:c.*2615T=	ENSP00000498237.1:n.*2615T=
ENST00000652016.1:c.*749T=	ENSP00000498267.1:n.*749T=
ENST00000652485.1:c.2565T=	ENSP00000498973.1:p.Ser855=
ENST00000378823.7:c.2532T=	ENSP00000368100.4:p.Ser844=
ENST00000423956.5:c.*718T=	ENSP00000390971.1:n.*718T=
ENST00000533482.5:c.*2158T=	ENSP00000431225.1:n.*2158T=
NM_005732.3:c.2532T=	NP_005723.2:p.Ser844=
NM_005732.4:c.2532T= MANE Select	NP_005723.2:p.Ser844=