Canonical Allele Identifier: CA3404941

Gene: RAD50

Linked Data

• ClinVar Variation Id: 230217
• ClinVar RCV Id: RCV000220496 ; RCV000764572
• dbSNP Id: rs371122101
• ExAC: 5:131911472 G / A
• gnomAD v2: 5-131911472-G-A
• gnomAD v3: 5-132575780-G-A
• gnomAD v4: 5-132575780-G-A
• MyVariant Identifiers: chr5:g.131911472G>A (hg19) ; chr5:g.132575780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132575780G>A , CM000667.2:g.132575780G>A	GRCh38
NC_000005.9:g.131911472G>A , CM000667.1:g.131911472G>A	GRCh37
NC_000005.8:g.131939371G>A	NCBI36
NG_021151.1:g.23857G>A
NG_021151.2:g.23804G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.217G>A MANE Select	ENSP00000368100.4:p.Ala73Thr
ENST00000638452.2:c.-81G>A	ENSP00000492349.2:n.-81G>A
ENST00000638504.1:n.294G>A
ENST00000638568.2:c.-81G>A	ENSP00000491158.2:n.-81G>A
ENST00000639899.1:n.377G>A
ENST00000640655.2:c.-81G>A	ENSP00000491596.2:n.-81G>A
ENST00000651160.1:c.217G>A	ENSP00000498829.1:p.Ala73Thr
ENST00000651541.1:c.-81G>A	ENSP00000498795.1:n.-81G>A
ENST00000651658.1:n.285G>A
ENST00000651723.1:c.*365G>A	ENSP00000498237.1:n.*365G>A
ENST00000652016.1:c.217G>A	ENSP00000498267.1:p.Ala73Thr
ENST00000652485.1:c.217G>A	ENSP00000498973.1:p.Ala73Thr
ENST00000378823.7:c.217G>A	ENSP00000368100.4:p.Ala73Thr
ENST00000416135.5:c.-81G>A	ENSP00000389515.1:n.-81G>A
ENST00000423956.5:c.217G>A	ENSP00000390971.1:p.Ala73Thr
ENST00000453394.5:c.217G>A	ENSP00000400049.1:p.Ala73Thr
ENST00000533482.5:c.217G>A	ENSP00000431225.1:p.Ala73Thr
NM_005732.3:c.217G>A	NP_005723.2:p.Ala73Thr
NM_005732.4:c.217G>A MANE Select	NP_005723.2:p.Ala73Thr