Canonical Allele Identifier: CA360933807

Gene: RAD50

Linked Data

• ClinVar Variation Id: 1738901
• ClinVar RCV Id: RCV002328112
• MyVariant Identifiers: chr5:g.131915065T>G (hg19) ; chr5:g.132579373T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579373T>G , CM000667.2:g.132579373T>G	GRCh38
NC_000005.9:g.131915065T>G , CM000667.1:g.131915065T>G	GRCh37
NC_000005.8:g.131942964T>G	NCBI36
NG_021151.1:g.27450T>G
NG_021151.2:g.27397T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.422T>G MANE Select	ENSP00000368100.4:p.Ile141Ser
ENST00000638452.2:c.125T>G	ENSP00000492349.2:p.Ile42Ser
ENST00000638504.1:n.442+3445T>G
ENST00000638568.2:c.125T>G	ENSP00000491158.2:p.Ile42Ser
ENST00000639899.1:n.582T>G
ENST00000640655.2:c.125T>G	ENSP00000491596.2:p.Ile42Ser
ENST00000651160.1:c.422T>G	ENSP00000498829.1:p.Ile141Ser
ENST00000651541.1:c.125T>G	ENSP00000498795.1:p.Ile42Ser
ENST00000651658.1:n.490T>G
ENST00000651723.1:c.*505T>G	ENSP00000498237.1:n.*505T>G
ENST00000652016.1:c.422T>G	ENSP00000498267.1:p.Ile141Ser
ENST00000652485.1:c.422T>G	ENSP00000498973.1:p.Ile141Ser
ENST00000378823.7:c.422T>G	ENSP00000368100.4:p.Ile141Ser
ENST00000416135.5:c.125T>G	ENSP00000389515.1:p.Ile42Ser
ENST00000423956.5:c.422T>G	ENSP00000390971.1:p.Ile141Ser
ENST00000453394.5:c.422T>G	ENSP00000400049.1:p.Ile141Ser
ENST00000533482.5:c.*48T>G	ENSP00000431225.1:n.*48T>G
NM_005732.3:c.422T>G	NP_005723.2:p.Ile141Ser
NM_005732.4:c.422T>G MANE Select	NP_005723.2:p.Ile141Ser