Canonical Allele Identifier: CA288195

Gene: RAD50

Linked Data

• ClinVar Variation Id: 127997
• ClinVar RCV Id: RCV000222369 ; RCV001781445
• dbSNP Id: rs587780150
• gnomAD v4: 5-132589778-C-T
• MyVariant Identifiers: chr5:g.131925470C>T (hg19) ; chr5:g.132589778C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589778C>T , CM000667.2:g.132589778C>T	GRCh38
NC_000005.9:g.131925470C>T , CM000667.1:g.131925470C>T	GRCh37
NC_000005.8:g.131953369C>T	NCBI36
NG_021151.1:g.37855C>T
NG_021151.2:g.37802C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.1393C>T MANE Select	ENSP00000368100.4:p.Gln465Ter
ENST00000638452.2:c.1096C>T	ENSP00000492349.2:p.Gln366Ter
ENST00000638504.1:n.1079C>T
ENST00000638568.2:c.1096C>T	ENSP00000491158.2:p.Gln366Ter
ENST00000639899.1:n.1912C>T
ENST00000640655.2:c.1096C>T	ENSP00000491596.2:p.Gln366Ter
ENST00000651160.1:c.1393C>T	ENSP00000498829.1:p.Gln465Ter
ENST00000651541.1:c.1096C>T	ENSP00000498795.1:p.Gln366Ter
ENST00000651658.1:n.1820C>T
ENST00000651723.1:c.*1476C>T	ENSP00000498237.1:n.*1476C>T
ENST00000652016.1:c.1393C>T	ENSP00000498267.1:p.Gln465Ter
ENST00000652485.1:c.1393C>T	ENSP00000498973.1:p.Gln465Ter
ENST00000378823.7:c.1393C>T	ENSP00000368100.4:p.Gln465Ter
ENST00000423956.5:c.1393C>T	ENSP00000390971.1:p.Gln465Ter
ENST00000453394.5:c.1393C>T	ENSP00000400049.1:p.Gln465Ter
ENST00000533482.5:c.*1019C>T	ENSP00000431225.1:n.*1019C>T
NM_005732.3:c.1393C>T	NP_005723.2:p.Gln465Ter
NM_005732.4:c.1393C>T MANE Select	NP_005723.2:p.Gln465Ter