Canonical Allele Identifier: CA1583229559

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609150_132609151delinsCA , CM000667.2:g.132609150_132609151delinsCA	GRCh38
NC_000005.9:g.131944842_131944843delinsCA , CM000667.1:g.131944842_131944843delinsCA	GRCh37
NC_000005.8:g.131972741_131972742delinsCA	NCBI36
NG_021151.1:g.57227_57228delinsCA
NG_021151.2:g.57174_57175delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2863_2864delinsCA MANE Select	ENSP00000368100.4:p.His955=
ENST00000638452.2:c.2566_2567delinsCA	ENSP00000492349.2:p.His856=
ENST00000638504.1:n.2471_2472delinsCA
ENST00000638568.2:c.2566_2567delinsCA	ENSP00000491158.2:p.His856=
ENST00000639899.1:n.3382_3383delinsCA
ENST00000640655.2:c.2566_2567delinsCA	ENSP00000491596.2:p.His856=
ENST00000651160.1:c.*1007_*1008delinsCA	ENSP00000498829.1:n.*1007_*1008delinsCA
ENST00000651723.1:c.*2946_*2947delinsCA	ENSP00000498237.1:n.*2946_*2947delinsCA
ENST00000378823.7:c.2863_2864delinsCA	ENSP00000368100.4:p.His955=
ENST00000423956.5:c.*1049_*1050delinsCA	ENSP00000390971.1:n.*1049_*1050delinsCA
ENST00000533482.5:c.*2489_*2490delinsCA	ENSP00000431225.1:n.*2489_*2490delinsCA
NM_005732.3:c.2863_2864delinsCA	NP_005723.2:p.His955=
NM_005732.4:c.2863_2864delinsCA MANE Select	NP_005723.2:p.His955=