Canonical Allele Identifier: CA1583225262

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132575879A= , CM000667.2:g.132575879A=	GRCh38
NC_000005.9:g.131911571A= , CM000667.1:g.131911571A=	GRCh37
NC_000005.8:g.131939470A=	NCBI36
NG_021151.1:g.23956A=
NG_021151.2:g.23903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.316A= MANE Select	ENSP00000368100.4:p.Ser106=
ENST00000638452.2:c.19A=	ENSP00000492349.2:p.Ser7=
ENST00000638504.1:n.393A=
ENST00000638568.2:c.19A=	ENSP00000491158.2:p.Ser7=
ENST00000639899.1:n.476A=
ENST00000640655.2:c.19A=	ENSP00000491596.2:p.Ser7=
ENST00000651160.1:c.316A=	ENSP00000498829.1:p.Ser106=
ENST00000651541.1:c.19A=	ENSP00000498795.1:p.Ser7=
ENST00000651658.1:n.384A=
ENST00000651723.1:c.*448+16A=	ENSP00000498237.1:n.*448+16A=
ENST00000652016.1:c.316A=	ENSP00000498267.1:p.Ser106=
ENST00000652485.1:c.316A=	ENSP00000498973.1:p.Ser106=
ENST00000378823.7:c.316A=	ENSP00000368100.4:p.Ser106=
ENST00000416135.5:c.19A=	ENSP00000389515.1:p.Ser7=
ENST00000423956.5:c.316A=	ENSP00000390971.1:p.Ser106=
ENST00000453394.5:c.316A=	ENSP00000400049.1:p.Ser106=
ENST00000533482.5:c.300+16A=	ENSP00000431225.1:n.300+16A=
NM_005732.3:c.316A=	NP_005723.2:p.Ser106=
NM_005732.4:c.316A= MANE Select	NP_005723.2:p.Ser106=