Canonical Allele Identifier: CA1583238153

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588808_132588809delinsAC , CM000667.2:g.132588808_132588809delinsAC	GRCh38
NC_000005.9:g.131924500_131924501delinsAC , CM000667.1:g.131924500_131924501delinsAC	GRCh37
NC_000005.8:g.131952399_131952400delinsAC	NCBI36
NG_021151.1:g.36885_36886delinsAC
NG_021151.2:g.36832_36833delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1173_1174delinsAC MANE Select	ENSP00000368100.4:p.Arg391=
ENST00000638452.2:c.876_877delinsAC	ENSP00000492349.2:p.Arg292=
ENST00000638504.1:n.859_860delinsAC
ENST00000638568.2:c.876_877delinsAC	ENSP00000491158.2:p.Arg292=
ENST00000639899.1:n.1692_1693delinsAC
ENST00000640655.2:c.876_877delinsAC	ENSP00000491596.2:p.Arg292=
ENST00000651160.1:c.1173_1174delinsAC	ENSP00000498829.1:p.Arg391=
ENST00000651541.1:c.876_877delinsAC	ENSP00000498795.1:p.Arg292=
ENST00000651658.1:n.1600_1601delinsAC
ENST00000651723.1:c.*1256_*1257delinsAC	ENSP00000498237.1:n.*1256_*1257delinsAC
ENST00000652016.1:c.1173_1174delinsAC	ENSP00000498267.1:p.Arg391=
ENST00000652485.1:c.1173_1174delinsAC	ENSP00000498973.1:p.Arg391=
ENST00000378823.7:c.1173_1174delinsAC	ENSP00000368100.4:p.Arg391=
ENST00000423956.5:c.1173_1174delinsAC	ENSP00000390971.1:p.Arg391=
ENST00000453394.5:c.1173_1174delinsAC	ENSP00000400049.1:p.Arg391=
ENST00000533482.5:c.*799_*800delinsAC	ENSP00000431225.1:n.*799_*800delinsAC
NM_005732.3:c.1173_1174delinsAC	NP_005723.2:p.Arg391=
NM_005732.4:c.1173_1174delinsAC MANE Select	NP_005723.2:p.Arg391=