Canonical Allele Identifier: CA360942276

Gene: RAD50

Linked Data

• ClinVar Variation Id: 856693
• ClinVar RCV Id: RCV001062206
• dbSNP Id: rs146370443
• MyVariant Identifiers: chr5:g.131924421G>C (hg19) ; chr5:g.132588729G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588729G>C , CM000667.2:g.132588729G>C	GRCh38
NC_000005.9:g.131924421G>C , CM000667.1:g.131924421G>C	GRCh37
NC_000005.8:g.131952320G>C	NCBI36
NG_021151.1:g.36806G>C
NG_021151.2:g.36753G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1094G>C MANE Select	ENSP00000368100.4:p.Arg365Pro
ENST00000638452.2:c.797G>C	ENSP00000492349.2:p.Arg266Pro
ENST00000638504.1:n.780G>C
ENST00000638568.2:c.797G>C	ENSP00000491158.2:p.Arg266Pro
ENST00000639899.1:n.1613G>C
ENST00000640655.2:c.797G>C	ENSP00000491596.2:p.Arg266Pro
ENST00000651160.1:c.1094G>C	ENSP00000498829.1:p.Arg365Pro
ENST00000651541.1:c.797G>C	ENSP00000498795.1:p.Arg266Pro
ENST00000651658.1:n.1521G>C
ENST00000651723.1:c.*1177G>C	ENSP00000498237.1:n.*1177G>C
ENST00000652016.1:c.1094G>C	ENSP00000498267.1:p.Arg365Pro
ENST00000652485.1:c.1094G>C	ENSP00000498973.1:p.Arg365Pro
ENST00000378823.7:c.1094G>C	ENSP00000368100.4:p.Arg365Pro
ENST00000423956.5:c.1094G>C	ENSP00000390971.1:p.Arg365Pro
ENST00000453394.5:c.1094G>C	ENSP00000400049.1:p.Arg365Pro
ENST00000487596.1:n.660G>C
ENST00000533482.5:c.*720G>C	ENSP00000431225.1:n.*720G>C
NM_005732.3:c.1094G>C	NP_005723.2:p.Arg365Pro
NM_005732.4:c.1094G>C MANE Select	NP_005723.2:p.Arg365Pro