Canonical Allele Identifier: CA360942774

Gene: RAD50

Linked Data

• ClinVar Variation Id: 486248
• ClinVar RCV Id: RCV000569375
• dbSNP Id: rs876659781
• MyVariant Identifiers: chr5:g.131924500A>T (hg19) ; chr5:g.132588808A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588808A>T , CM000667.2:g.132588808A>T	GRCh38
NC_000005.9:g.131924500A>T , CM000667.1:g.131924500A>T	GRCh37
NC_000005.8:g.131952399A>T	NCBI36
NG_021151.1:g.36885A>T
NG_021151.2:g.36832A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1173A>T MANE Select	ENSP00000368100.4:p.Arg391Ser
ENST00000638452.2:c.876A>T	ENSP00000492349.2:p.Arg292Ser
ENST00000638504.1:n.859A>T
ENST00000638568.2:c.876A>T	ENSP00000491158.2:p.Arg292Ser
ENST00000639899.1:n.1692A>T
ENST00000640655.2:c.876A>T	ENSP00000491596.2:p.Arg292Ser
ENST00000651160.1:c.1173A>T	ENSP00000498829.1:p.Arg391Ser
ENST00000651541.1:c.876A>T	ENSP00000498795.1:p.Arg292Ser
ENST00000651658.1:n.1600A>T
ENST00000651723.1:c.*1256A>T	ENSP00000498237.1:n.*1256A>T
ENST00000652016.1:c.1173A>T	ENSP00000498267.1:p.Arg391Ser
ENST00000652485.1:c.1173A>T	ENSP00000498973.1:p.Arg391Ser
ENST00000378823.7:c.1173A>T	ENSP00000368100.4:p.Arg391Ser
ENST00000423956.5:c.1173A>T	ENSP00000390971.1:p.Arg391Ser
ENST00000453394.5:c.1173A>T	ENSP00000400049.1:p.Arg391Ser
ENST00000533482.5:c.*799A>T	ENSP00000431225.1:n.*799A>T
NM_005732.3:c.1173A>T	NP_005723.2:p.Arg391Ser
NM_005732.4:c.1173A>T MANE Select	NP_005723.2:p.Arg391Ser