Canonical Allele Identifier: CA2675217827

Gene: RAD50

Linked Data

• gnomAD v4: 5-132609240-TTGTATTTTTATTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609244_132609257del , CM000667.2:g.132609244_132609257del	GRCh38
NC_000005.9:g.131944936_131944949del , CM000667.1:g.131944936_131944949del	GRCh37
NC_000005.8:g.131972835_131972848del	NCBI36
NG_021151.1:g.57321_57334del
NG_021151.2:g.57268_57281del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2922+35_2923-26del MANE Select	ENSP00000368100.4:n.2922+35_2923-26del
ENST00000638452.2:c.2625+35_2626-26del	ENSP00000492349.2:n.2625+35_2626-26del
ENST00000638504.1:n.2530+35_2531-26del
ENST00000638568.2:c.2625+35_2626-26del	ENSP00000491158.2:n.2625+35_2626-26del
ENST00000639899.1:n.3441+35_3442-26del
ENST00000640655.2:c.2625+35_2626-26del	ENSP00000491596.2:n.2625+35_2626-26del
ENST00000651160.1:c.*1066+35_*1067-26del	ENSP00000498829.1:n.*1066+35_*1067-26del
ENST00000651723.1:c.*3005+35_*3006-26del	ENSP00000498237.1:n.*3005+35_*3006-26del
ENST00000378823.7:c.2922+35_2923-26del	ENSP00000368100.4:n.2922+35_2923-26del
ENST00000423956.5:c.*1108+35_*1109-26del	ENSP00000390971.1:n.*1108+35_*1109-26del
ENST00000533482.5:c.*2548+35_*2549-26del	ENSP00000431225.1:n.*2548+35_*2549-26del
NM_005732.3:c.2922+35_2923-26del	NP_005723.2:n.2922+35_2923-26del
NM_005732.4:c.2922+35_2923-26del MANE Select	NP_005723.2:n.2922+35_2923-26del