Canonical Allele Identifier: CA562778033

Gene: RAD50

Linked Data

• dbSNP Id: rs1345358774
• gnomAD v2: 5-131954228-G-A
• gnomAD v3: 5-132618536-G-A
• gnomAD v4: 5-132618536-G-A
• MyVariant Identifiers: chr5:g.131954228G>A (hg19) ; chr5:g.132618536G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618536G>A , CM000667.2:g.132618536G>A	GRCh38
NC_000005.9:g.131954228G>A , CM000667.1:g.131954228G>A	GRCh37
NC_000005.8:g.131982127G>A	NCBI36
NG_021151.1:g.66613G>A
NG_021151.2:g.66560G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3389+242G>A MANE Select	ENSP00000368100.4:n.3389+242G>A
ENST00000638452.2:c.3092+242G>A	ENSP00000492349.2:n.3092+242G>A
ENST00000638504.1:n.2997+242G>A
ENST00000638568.2:c.3092+242G>A	ENSP00000491158.2:n.3092+242G>A
ENST00000639899.1:n.3908+242G>A
ENST00000640655.2:c.3092+242G>A	ENSP00000491596.2:n.3092+242G>A
ENST00000651249.1:c.225+242G>A
ENST00000378823.7:c.3389+242G>A	ENSP00000368100.4:n.3389+242G>A
ENST00000455677.1:c.24+242G>A
ENST00000533482.5:c.*3015+242G>A	ENSP00000431225.1:n.*3015+242G>A
NM_005732.3:c.3389+242G>A	NP_005723.2:n.3389+242G>A
NM_005732.4:c.3389+242G>A MANE Select	NP_005723.2:n.3389+242G>A