Canonical Allele Identifier: CA360955880

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131939722G>C (hg19) ; chr5:g.132604030G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604030G>C , CM000667.2:g.132604030G>C	GRCh38
NC_000005.9:g.131939722G>C , CM000667.1:g.131939722G>C	GRCh37
NC_000005.8:g.131967621G>C	NCBI36
NG_021151.1:g.52107G>C
NG_021151.2:g.52054G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2508G>C MANE Select	ENSP00000368100.4:p.Gln836His
ENST00000638452.2:c.2211G>C	ENSP00000492349.2:p.Gln737His
ENST00000638504.1:n.2116G>C
ENST00000638568.2:c.2211G>C	ENSP00000491158.2:p.Gln737His
ENST00000639899.1:n.3027G>C
ENST00000640655.2:c.2211G>C	ENSP00000491596.2:p.Gln737His
ENST00000651160.1:c.*652G>C	ENSP00000498829.1:n.*652G>C
ENST00000651658.1:n.3051G>C
ENST00000651723.1:c.*2591G>C	ENSP00000498237.1:n.*2591G>C
ENST00000652016.1:c.*725G>C	ENSP00000498267.1:n.*725G>C
ENST00000652485.1:c.2541G>C	ENSP00000498973.1:p.Gln847His
ENST00000378823.7:c.2508G>C	ENSP00000368100.4:p.Gln836His
ENST00000423956.5:c.*694G>C	ENSP00000390971.1:n.*694G>C
ENST00000533482.5:c.*2134G>C	ENSP00000431225.1:n.*2134G>C
NM_005732.3:c.2508G>C	NP_005723.2:p.Gln836His
NM_005732.4:c.2508G>C MANE Select	NP_005723.2:p.Gln836His