Canonical Allele Identifier: CA2675215682

Gene: RAD50

Linked Data

• gnomAD v4: 5-132557094-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557098del , CM000667.2:g.132557098del	GRCh38
NC_000005.9:g.131892790del , CM000667.1:g.131892790del	GRCh37
NC_000005.8:g.131920689del	NCBI36
NG_021151.1:g.5175del
NG_021151.2:g.5122del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.-227del MANE Select	ENSP00000368100.4:n.-227del
ENST00000638452.2:c.-168-2186del	ENSP00000492349.2:n.-168-2186del
ENST00000638504.1:n.207-2186del
ENST00000638568.2:c.-169+625del	ENSP00000491158.2:n.-169+625del
ENST00000639899.1:n.290-2186del
ENST00000640655.2:c.-168-2186del	ENSP00000491596.2:n.-168-2186del
ENST00000651160.1:c.-227del	ENSP00000498829.1:n.-227del
ENST00000651541.1:c.-169+89del	ENSP00000498795.1:n.-169+89del
ENST00000652016.1:c.-227del	ENSP00000498267.1:n.-227del
ENST00000652485.1:c.-227del	ENSP00000498973.1:n.-227del
ENST00000378823.7:c.-227del	ENSP00000368100.4:n.-227del
ENST00000416135.5:c.-169+625del	ENSP00000389515.1:n.-169+625del
ENST00000533482.5:c.-227del	ENSP00000431225.1:n.-227del
NM_005732.3:c.-227del	NP_005723.2:n.-227del
NM_005732.4:c.-227del MANE Select	NP_005723.2:n.-227del