Canonical Allele Identifier: CA2675215639

Gene: RAD50

Linked Data

• gnomAD v4: 5-132557058-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557058C>A , CM000667.2:g.132557058C>A	GRCh38
NC_000005.9:g.131892750C>A , CM000667.1:g.131892750C>A	GRCh37
NC_000005.8:g.131920649C>A	NCBI36
NG_021151.1:g.5135C>A
NG_021151.2:g.5082C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.-267C>A MANE Select	ENSP00000368100.4:n.-267C>A
ENST00000638452.2:c.-168-2226C>A	ENSP00000492349.2:n.-168-2226C>A
ENST00000638504.1:n.207-2226C>A
ENST00000638568.2:c.-169+585C>A	ENSP00000491158.2:n.-169+585C>A
ENST00000639899.1:n.290-2226C>A
ENST00000640655.2:c.-168-2226C>A	ENSP00000491596.2:n.-168-2226C>A
ENST00000651160.1:c.-267C>A	ENSP00000498829.1:n.-267C>A
ENST00000651541.1:c.-169+49C>A	ENSP00000498795.1:n.-169+49C>A
ENST00000652016.1:c.-267C>A	ENSP00000498267.1:n.-267C>A
ENST00000652485.1:c.-267C>A	ENSP00000498973.1:n.-267C>A
ENST00000378823.7:c.-267C>A	ENSP00000368100.4:n.-267C>A
ENST00000416135.5:c.-169+585C>A	ENSP00000389515.1:n.-169+585C>A
ENST00000533482.5:c.-267C>A	ENSP00000431225.1:n.-267C>A
NM_005732.3:c.-267C>A	NP_005723.2:n.-267C>A
NM_005732.4:c.-267C>A MANE Select	NP_005723.2:n.-267C>A