Canonical Allele Identifier: CA1583238404

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588909_132588910delinsAT , CM000667.2:g.132588909_132588910delinsAT	GRCh38
NC_000005.9:g.131924601_131924602delinsAT , CM000667.1:g.131924601_131924602delinsAT	GRCh37
NC_000005.8:g.131952500_131952501delinsAT	NCBI36
NG_021151.1:g.36986_36987delinsAT
NG_021151.2:g.36933_36934delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1245+29_1245+30delinsAT MANE Select	ENSP00000368100.4:n.1245+29_1245+30delinsAT
ENST00000638452.2:c.948+29_948+30delinsAT	ENSP00000492349.2:n.948+29_948+30delinsAT
ENST00000638504.1:n.931+29_931+30delinsAT
ENST00000638568.2:c.948+29_948+30delinsAT	ENSP00000491158.2:n.948+29_948+30delinsAT
ENST00000639899.1:n.1764+29_1764+30delinsAT
ENST00000640655.2:c.948+29_948+30delinsAT	ENSP00000491596.2:n.948+29_948+30delinsAT
ENST00000651160.1:c.1245+29_1245+30delinsAT	ENSP00000498829.1:n.1245+29_1245+30delinsAT
ENST00000651541.1:c.948+29_948+30delinsAT	ENSP00000498795.1:n.948+29_948+30delinsAT
ENST00000651658.1:n.1672+29_1672+30delinsAT
ENST00000651723.1:c.*1328+29_*1328+30delinsAT	ENSP00000498237.1:n.*1328+29_*1328+30delinsAT
ENST00000652016.1:c.1245+29_1245+30delinsAT	ENSP00000498267.1:n.1245+29_1245+30delinsAT
ENST00000652485.1:c.1245+29_1245+30delinsAT	ENSP00000498973.1:n.1245+29_1245+30delinsAT
ENST00000378823.7:c.1245+29_1245+30delinsAT	ENSP00000368100.4:n.1245+29_1245+30delinsAT
ENST00000423956.5:c.1245+29_1245+30delinsAT	ENSP00000390971.1:n.1245+29_1245+30delinsAT
ENST00000453394.5:c.1245+29_1245+30delinsAT	ENSP00000400049.1:n.1245+29_1245+30delinsAT
ENST00000533482.5:c.*871+29_*871+30delinsAT	ENSP00000431225.1:n.*871+29_*871+30delinsAT
NM_005732.3:c.1245+29_1245+30delinsAT	NP_005723.2:n.1245+29_1245+30delinsAT
NM_005732.4:c.1245+29_1245+30delinsAT MANE Select	NP_005723.2:n.1245+29_1245+30delinsAT