Canonical Allele Identifier: CA446362171

Gene: RAD50

Linked Data

• ClinVar Variation Id: 2451437
• ClinVar RCV Id: RCV003182453
• MyVariant Identifiers: chr5:g.131930717A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595025A>G , CM000667.2:g.132595025A>G	GRCh38
NC_000005.9:g.131930717A>G , CM000667.1:g.131930717A>G	GRCh37
NC_000005.8:g.131958616A>G	NCBI36
NG_021151.1:g.43102A>G
NG_021151.2:g.43049A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1950A>G MANE Select	ENSP00000368100.4:p.Glu650=
ENST00000638452.2:c.1653A>G	ENSP00000492349.2:p.Glu551=
ENST00000638504.1:n.1480-79A>G
ENST00000638568.2:c.1653A>G	ENSP00000491158.2:p.Glu551=
ENST00000639899.1:n.2469A>G
ENST00000640655.2:c.1653A>G	ENSP00000491596.2:p.Glu551=
ENST00000651160.1:c.*16-79A>G	ENSP00000498829.1:n.*16-79A>G
ENST00000651658.1:n.2493A>G
ENST00000651723.1:c.*2033A>G	ENSP00000498237.1:n.*2033A>G
ENST00000652016.1:c.*89-79A>G	ENSP00000498267.1:n.*89-79A>G
ENST00000652485.1:c.1983A>G	ENSP00000498973.1:p.Glu661=
ENST00000378823.7:c.1950A>G	ENSP00000368100.4:p.Glu650=
ENST00000423956.5:c.*136A>G	ENSP00000390971.1:n.*136A>G
ENST00000453394.5:c.1767A>G	ENSP00000400049.1:p.Glu589=
ENST00000533482.5:c.*1576A>G	ENSP00000431225.1:n.*1576A>G
NM_005732.3:c.1950A>G	NP_005723.2:p.Glu650=
NM_005732.4:c.1950A>G MANE Select	NP_005723.2:p.Glu650=