Canonical Allele Identifier: CA2675217832

Gene: RAD50

Linked Data

• gnomAD v4: 5-132609259-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609259_132609260insA , CM000667.2:g.132609259_132609260insA	GRCh38
NC_000005.9:g.131944951_131944952insA , CM000667.1:g.131944951_131944952insA	GRCh37
NC_000005.8:g.131972850_131972851insA	NCBI36
NG_021151.1:g.57336_57337insA
NG_021151.2:g.57283_57284insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2923-24_2923-23insA MANE Select	ENSP00000368100.4:n.2923-24_2923-23insA
ENST00000638452.2:c.2626-24_2626-23insA	ENSP00000492349.2:n.2626-24_2626-23insA
ENST00000638504.1:n.2531-24_2531-23insA
ENST00000638568.2:c.2626-24_2626-23insA	ENSP00000491158.2:n.2626-24_2626-23insA
ENST00000639899.1:n.3442-24_3442-23insA
ENST00000640655.2:c.2626-24_2626-23insA	ENSP00000491596.2:n.2626-24_2626-23insA
ENST00000651160.1:c.*1067-24_*1067-23insA	ENSP00000498829.1:n.*1067-24_*1067-23insA...
ENST00000651723.1:c.*3006-24_*3006-23insA	ENSP00000498237.1:n.*3006-24_*3006-23insA...
ENST00000378823.7:c.2923-24_2923-23insA	ENSP00000368100.4:n.2923-24_2923-23insA
ENST00000423956.5:c.*1109-24_*1109-23insA	ENSP00000390971.1:n.*1109-24_*1109-23insA...
ENST00000533482.5:c.*2549-24_*2549-23insA	ENSP00000431225.1:n.*2549-24_*2549-23insA...
NM_005732.3:c.2923-24_2923-23insA	NP_005723.2:n.2923-24_2923-23insA
NM_005732.4:c.2923-24_2923-23insA MANE Select	NP_005723.2:n.2923-24_2923-23insA