Canonical Allele Identifier: CA2675217829

Gene: RAD50

Linked Data

• gnomAD v4: 5-132609246-TTTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609249_132609252del , CM000667.2:g.132609249_132609252del	GRCh38
NC_000005.9:g.131944941_131944944del , CM000667.1:g.131944941_131944944del	GRCh37
NC_000005.8:g.131972840_131972843del	NCBI36
NG_021151.1:g.57326_57329del
NG_021151.2:g.57273_57276del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2923-34_2923-31del MANE Select	ENSP00000368100.4:n.2923-34_2923-31del
ENST00000638452.2:c.2626-34_2626-31del	ENSP00000492349.2:n.2626-34_2626-31del
ENST00000638504.1:n.2531-34_2531-31del
ENST00000638568.2:c.2626-34_2626-31del	ENSP00000491158.2:n.2626-34_2626-31del
ENST00000639899.1:n.3442-34_3442-31del
ENST00000640655.2:c.2626-34_2626-31del	ENSP00000491596.2:n.2626-34_2626-31del
ENST00000651160.1:c.*1067-34_*1067-31del	ENSP00000498829.1:n.*1067-34_*1067-31del
ENST00000651723.1:c.*3006-34_*3006-31del	ENSP00000498237.1:n.*3006-34_*3006-31del
ENST00000378823.7:c.2923-34_2923-31del	ENSP00000368100.4:n.2923-34_2923-31del
ENST00000423956.5:c.*1109-34_*1109-31del	ENSP00000390971.1:n.*1109-34_*1109-31del
ENST00000533482.5:c.*2549-34_*2549-31del	ENSP00000431225.1:n.*2549-34_*2549-31del
NM_005732.3:c.2923-34_2923-31del	NP_005723.2:n.2923-34_2923-31del
NM_005732.4:c.2923-34_2923-31del MANE Select	NP_005723.2:n.2923-34_2923-31del