Canonical Allele Identifier: CA360948613

Gene: RAD50

Linked Data

• ClinVar Variation Id: 1469807
• ClinVar RCV Id: RCV001961757
• dbSNP Id: rs2149843787
• MyVariant Identifiers: chr5:g.131930727A>C (hg19) ; chr5:g.132595035A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595035A>C , CM000667.2:g.132595035A>C	GRCh38
NC_000005.9:g.131930727A>C , CM000667.1:g.131930727A>C	GRCh37
NC_000005.8:g.131958626A>C	NCBI36
NG_021151.1:g.43112A>C
NG_021151.2:g.43059A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1960A>C MANE Select	ENSP00000368100.4:p.Lys654Gln
ENST00000638452.2:c.1663A>C	ENSP00000492349.2:p.Lys555Gln
ENST00000638504.1:n.1480-69A>C
ENST00000638568.2:c.1663A>C	ENSP00000491158.2:p.Lys555Gln
ENST00000639899.1:n.2479A>C
ENST00000640655.2:c.1663A>C	ENSP00000491596.2:p.Lys555Gln
ENST00000651160.1:c.*16-69A>C	ENSP00000498829.1:n.*16-69A>C
ENST00000651658.1:n.2503A>C
ENST00000651723.1:c.*2043A>C	ENSP00000498237.1:n.*2043A>C
ENST00000652016.1:c.*89-69A>C	ENSP00000498267.1:n.*89-69A>C
ENST00000652485.1:c.1993A>C	ENSP00000498973.1:p.Lys665Gln
ENST00000378823.7:c.1960A>C	ENSP00000368100.4:p.Lys654Gln
ENST00000423956.5:c.*146A>C	ENSP00000390971.1:n.*146A>C
ENST00000453394.5:c.1777A>C	ENSP00000400049.1:p.Lys593Gln
ENST00000533482.5:c.*1586A>C	ENSP00000431225.1:n.*1586A>C
NM_005732.3:c.1960A>C	NP_005723.2:p.Lys654Gln
NM_005732.4:c.1960A>C MANE Select	NP_005723.2:p.Lys654Gln