Canonical Allele Identifier: CA1583226901

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579414A= , CM000667.2:g.132579414A=	GRCh38
NC_000005.9:g.131915106A= , CM000667.1:g.131915106A=	GRCh37
NC_000005.8:g.131943005A=	NCBI36
NG_021151.1:g.27491A=
NG_021151.2:g.27438A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.463A= MANE Select	ENSP00000368100.4:p.Ile155=
ENST00000638452.2:c.166A=	ENSP00000492349.2:p.Ile56=
ENST00000638504.1:n.442+3486A=
ENST00000638568.2:c.166A=	ENSP00000491158.2:p.Ile56=
ENST00000639899.1:n.623A=
ENST00000640655.2:c.166A=	ENSP00000491596.2:p.Ile56=
ENST00000651160.1:c.463A=	ENSP00000498829.1:p.Ile155=
ENST00000651541.1:c.166A=	ENSP00000498795.1:p.Ile56=
ENST00000651658.1:n.531A=
ENST00000651723.1:c.*546A=	ENSP00000498237.1:n.*546A=
ENST00000652016.1:c.463A=	ENSP00000498267.1:p.Ile155=
ENST00000652485.1:c.463A=	ENSP00000498973.1:p.Ile155=
ENST00000378823.7:c.463A=	ENSP00000368100.4:p.Ile155=
ENST00000416135.5:c.166A=	ENSP00000389515.1:p.Ile56=
ENST00000423956.5:c.463A=	ENSP00000390971.1:p.Ile155=
ENST00000453394.5:c.463A=	ENSP00000400049.1:p.Ile155=
ENST00000533482.5:c.*89A=	ENSP00000431225.1:n.*89A=
NM_005732.3:c.463A=	NP_005723.2:p.Ile155=
NM_005732.4:c.463A= MANE Select	NP_005723.2:p.Ile155=