Canonical Allele Identifier: CA804000166

Gene: RAD50 TH2LCRR

Linked Data

• dbSNP Id: rs1214430039
• gnomAD v3: 5-132641382-A-C
• gnomAD v4: 5-132641382-A-C
• MyVariant Identifiers: chr5:g.131977074A>C (hg19) ; chr5:g.132641382A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132641382A>C , CM000667.2:g.132641382A>C	GRCh38
NC_000005.9:g.131977074A>C , CM000667.1:g.131977074A>C	GRCh37
NC_000005.8:g.132004973A>C	NCBI36
NG_021151.1:g.89459A>C
NG_021151.2:g.89406A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3752+577A>C (RAD50) MANE Select	ENSP00000368100.4:n.3752+577A>C
ENST00000638452.2:c.3455+577A>C	ENSP00000492349.2:n.3455+577A>C
ENST00000638504.1:n.3360+577A>C
ENST00000638568.2:c.3455+577A>C	ENSP00000491158.2:n.3455+577A>C
ENST00000639899.1:n.4271+577A>C
ENST00000640655.2:c.3455+577A>C	ENSP00000491596.2:n.3455+577A>C
ENST00000651249.1:c.588+577A>C (RAD50)
ENST00000378823.7:c.3752+577A>C (RAD50)	ENSP00000368100.4:n.3752+577A>C
ENST00000455677.1:c.387+577A>C (RAD50)
ENST00000533482.5:c.*3378+577A>C (RAD50)	ENSP00000431225.1:n.*3378+577A>C
NM_005732.3:c.3752+577A>C (RAD50)	NP_005723.2:n.3752+577A>C
NR_132124.1:n.45+364T>G (TH2LCRR)
NR_132125.1:n.189+816T>G (TH2LCRR)
NR_132126.1:n.175-3117T>G (TH2LCRR)
XR_427771.1:n.426+364T>G (TH2LCRR)
NM_005732.4:c.3752+577A>C (RAD50) MANE Select	NP_005723.2:n.3752+577A>C