Canonical Allele Identifier: CA1583233432

Gene: RAD50

Linked Data

• dbSNP Id: rs1751206434
• gnomAD v4: 5-132618014-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618014T>G , CM000667.2:g.132618014T>G	GRCh38
NC_000005.9:g.131953706T>G , CM000667.1:g.131953706T>G	GRCh37
NC_000005.8:g.131981605T>G	NCBI36
NG_021151.1:g.66091T>G
NG_021151.2:g.66038T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3165-56T>G MANE Select	ENSP00000368100.4:n.3165-56T>G
ENST00000638452.2:c.2868-56T>G	ENSP00000492349.2:n.2868-56T>G
ENST00000638504.1:n.2773-56T>G
ENST00000638568.2:c.2868-56T>G	ENSP00000491158.2:n.2868-56T>G
ENST00000639899.1:n.3684-56T>G
ENST00000640655.2:c.2868-56T>G	ENSP00000491596.2:n.2868-56T>G
ENST00000378823.7:c.3165-56T>G	ENSP00000368100.4:n.3165-56T>G
ENST00000533482.5:c.*2791-56T>G	ENSP00000431225.1:n.*2791-56T>G
NM_005732.3:c.3165-56T>G	NP_005723.2:n.3165-56T>G
NM_005732.4:c.3165-56T>G MANE Select	NP_005723.2:n.3165-56T>G