Canonical Allele Identifier: CA360930884

Gene: RAD50

Linked Data

• ClinVar Variation Id: 1447522
• ClinVar RCV Id: RCV001979865
• dbSNP Id: rs2149836428
• MyVariant Identifiers: chr5:g.131911544C>T (hg19) ; chr5:g.132575852C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132575852C>T , CM000667.2:g.132575852C>T	GRCh38
NC_000005.9:g.131911544C>T , CM000667.1:g.131911544C>T	GRCh37
NC_000005.8:g.131939443C>T	NCBI36
NG_021151.1:g.23929C>T
NG_021151.2:g.23876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.289C>T MANE Select	ENSP00000368100.4:p.Gln97Ter
ENST00000638452.2:c.-9C>T	ENSP00000492349.2:n.-9C>T
ENST00000638504.1:n.366C>T
ENST00000638568.2:c.-9C>T	ENSP00000491158.2:n.-9C>T
ENST00000639899.1:n.449C>T
ENST00000640655.2:c.-9C>T	ENSP00000491596.2:n.-9C>T
ENST00000651160.1:c.289C>T	ENSP00000498829.1:p.Gln97Ter
ENST00000651541.1:c.-9C>T	ENSP00000498795.1:n.-9C>T
ENST00000651658.1:n.357C>T
ENST00000651723.1:c.*437C>T	ENSP00000498237.1:n.*437C>T
ENST00000652016.1:c.289C>T	ENSP00000498267.1:p.Gln97Ter
ENST00000652485.1:c.289C>T	ENSP00000498973.1:p.Gln97Ter
ENST00000378823.7:c.289C>T	ENSP00000368100.4:p.Gln97Ter
ENST00000416135.5:c.-9C>T	ENSP00000389515.1:n.-9C>T
ENST00000423956.5:c.289C>T	ENSP00000390971.1:p.Gln97Ter
ENST00000453394.5:c.289C>T	ENSP00000400049.1:p.Gln97Ter
ENST00000533482.5:c.289C>T	ENSP00000431225.1:p.Gln97Ter
NM_005732.3:c.289C>T	NP_005723.2:p.Gln97Ter
NM_005732.4:c.289C>T MANE Select	NP_005723.2:p.Gln97Ter