Canonical Allele Identifier: CA127265963

Gene: RAD50

Linked Data

• dbSNP Id: rs905651838
• gnomAD v3: 5-132618470-C-T
• gnomAD v4: 5-132618470-C-T
• MyVariant Identifiers: chr5:g.131954162C>T (hg19) ; chr5:g.132618470C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618470C>T , CM000667.2:g.132618470C>T	GRCh38
NC_000005.9:g.131954162C>T , CM000667.1:g.131954162C>T	GRCh37
NC_000005.8:g.131982061C>T	NCBI36
NG_021151.1:g.66547C>T
NG_021151.2:g.66494C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3389+176C>T MANE Select	ENSP00000368100.4:n.3389+176C>T
ENST00000638452.2:c.3092+176C>T	ENSP00000492349.2:n.3092+176C>T
ENST00000638504.1:n.2997+176C>T
ENST00000638568.2:c.3092+176C>T	ENSP00000491158.2:n.3092+176C>T
ENST00000639899.1:n.3908+176C>T
ENST00000640655.2:c.3092+176C>T	ENSP00000491596.2:n.3092+176C>T
ENST00000651249.1:c.225+176C>T
ENST00000378823.7:c.3389+176C>T	ENSP00000368100.4:n.3389+176C>T
ENST00000455677.1:c.24+176C>T
ENST00000533482.5:c.*3015+176C>T	ENSP00000431225.1:n.*3015+176C>T
NM_005732.3:c.3389+176C>T	NP_005723.2:n.3389+176C>T
NM_005732.4:c.3389+176C>T MANE Select	NP_005723.2:n.3389+176C>T