Canonical Allele Identifier: CA360943546

Gene: RAD50

Linked Data

• ClinVar Variation Id: 484722
• ClinVar RCV Id: RCV000568468
• dbSNP Id: rs1554098297
• MyVariant Identifiers: chr5:g.131925324A>G (hg19) ; chr5:g.132589632A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589632A>G , CM000667.2:g.132589632A>G	GRCh38
NC_000005.9:g.131925324A>G , CM000667.1:g.131925324A>G	GRCh37
NC_000005.8:g.131953223A>G	NCBI36
NG_021151.1:g.37709A>G
NG_021151.2:g.37656A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1247A>G MANE Select	ENSP00000368100.4:p.Asn416Ser
ENST00000638452.2:c.950A>G	ENSP00000492349.2:p.Asn317Ser
ENST00000638504.1:n.933A>G
ENST00000638568.2:c.950A>G	ENSP00000491158.2:p.Asn317Ser
ENST00000639899.1:n.1766A>G
ENST00000640655.2:c.950A>G	ENSP00000491596.2:p.Asn317Ser
ENST00000651160.1:c.1247A>G	ENSP00000498829.1:p.Asn416Ser
ENST00000651541.1:c.950A>G	ENSP00000498795.1:p.Asn317Ser
ENST00000651658.1:n.1674A>G
ENST00000651723.1:c.*1330A>G	ENSP00000498237.1:n.*1330A>G
ENST00000652016.1:c.1247A>G	ENSP00000498267.1:p.Asn416Ser
ENST00000652485.1:c.1247A>G	ENSP00000498973.1:p.Asn416Ser
ENST00000378823.7:c.1247A>G	ENSP00000368100.4:p.Asn416Ser
ENST00000423956.5:c.1247A>G	ENSP00000390971.1:p.Asn416Ser
ENST00000453394.5:c.1247A>G	ENSP00000400049.1:p.Asn416Ser
ENST00000533482.5:c.*873A>G	ENSP00000431225.1:n.*873A>G
NM_005732.3:c.1247A>G	NP_005723.2:p.Asn416Ser
NM_005732.4:c.1247A>G MANE Select	NP_005723.2:p.Asn416Ser