Canonical Allele Identifier: CA1583241857

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594995T= , CM000667.2:g.132594995T=	GRCh38
NC_000005.9:g.131930687T= , CM000667.1:g.131930687T=	GRCh37
NC_000005.8:g.131958586T=	NCBI36
NG_021151.1:g.43072T=
NG_021151.2:g.43019T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1920T= MANE Select	ENSP00000368100.4:p.Ser640=
ENST00000638452.2:c.1623T=	ENSP00000492349.2:p.Ser541=
ENST00000638504.1:n.1480-109T=
ENST00000638568.2:c.1623T=	ENSP00000491158.2:p.Ser541=
ENST00000639899.1:n.2439T=
ENST00000640655.2:c.1623T=	ENSP00000491596.2:p.Ser541=
ENST00000651160.1:c.*16-109T=	ENSP00000498829.1:n.*16-109T=
ENST00000651658.1:n.2463T=
ENST00000651723.1:c.*2003T=	ENSP00000498237.1:n.*2003T=
ENST00000652016.1:c.*89-109T=	ENSP00000498267.1:n.*89-109T=
ENST00000652485.1:c.1953T=	ENSP00000498973.1:p.Ser651=
ENST00000378823.7:c.1920T=	ENSP00000368100.4:p.Ser640=
ENST00000423956.5:c.*106T=	ENSP00000390971.1:n.*106T=
ENST00000453394.5:c.1737T=	ENSP00000400049.1:p.Ser579=
ENST00000533482.5:c.*1546T=	ENSP00000431225.1:n.*1546T=
NM_005732.3:c.1920T=	NP_005723.2:p.Ser640=
NM_005732.4:c.1920T= MANE Select	NP_005723.2:p.Ser640=