Canonical Allele Identifier: CA2578402444

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132559226del , CM000667.2:g.132559226del	GRCh38
NC_000005.9:g.131894918del , CM000667.1:g.131894918del	GRCh37
NC_000005.8:g.131922817del	NCBI36
NG_021151.1:g.7303del
NG_021151.2:g.7250del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.130-58del MANE Select	ENSP00000368100.4:n.130-58del
ENST00000638452.2:c.-168-58del	ENSP00000492349.2:n.-168-58del
ENST00000638504.1:n.207-58del
ENST00000638568.2:c.-168-58del	ENSP00000491158.2:n.-168-58del
ENST00000639899.1:n.290-58del
ENST00000640655.2:c.-168-58del	ENSP00000491596.2:n.-168-58del
ENST00000651160.1:c.130-58del	ENSP00000498829.1:n.130-58del
ENST00000651541.1:c.-168-58del	ENSP00000498795.1:n.-168-58del
ENST00000651658.1:n.198-58del
ENST00000651723.1:c.*278-58del	ENSP00000498237.1:n.*278-58del
ENST00000652016.1:c.130-58del	ENSP00000498267.1:n.130-58del
ENST00000652485.1:c.130-58del	ENSP00000498973.1:n.130-58del
ENST00000378823.7:c.130-58del	ENSP00000368100.4:n.130-58del
ENST00000416135.5:c.-168-58del	ENSP00000389515.1:n.-168-58del
ENST00000423956.5:c.130-58del	ENSP00000390971.1:n.130-58del
ENST00000453394.5:c.130-58del	ENSP00000400049.1:n.130-58del
ENST00000533482.5:c.130-58del	ENSP00000431225.1:n.130-58del
NM_005732.3:c.130-58del	NP_005723.2:n.130-58del
NM_005732.4:c.130-58del MANE Select	NP_005723.2:n.130-58del