Canonical Allele Identifier: CA360947614

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930600A>G (hg19) ; chr5:g.132594908A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594908A>G , CM000667.2:g.132594908A>G	GRCh38
NC_000005.9:g.131930600A>G , CM000667.1:g.131930600A>G	GRCh37
NC_000005.8:g.131958499A>G	NCBI36
NG_021151.1:g.42985A>G
NG_021151.2:g.42932A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1833A>G MANE Select	ENSP00000368100.4:p.Ile611Met
ENST00000638452.2:c.1536A>G	ENSP00000492349.2:p.Ile512Met
ENST00000638504.1:n.1480-196A>G
ENST00000638568.2:c.1536A>G	ENSP00000491158.2:p.Ile512Met
ENST00000639899.1:n.2352A>G
ENST00000640655.2:c.1536A>G	ENSP00000491596.2:p.Ile512Met
ENST00000651160.1:c.*16-196A>G	ENSP00000498829.1:n.*16-196A>G
ENST00000651658.1:n.2376A>G
ENST00000651723.1:c.*1916A>G	ENSP00000498237.1:n.*1916A>G
ENST00000652016.1:c.*89-196A>G	ENSP00000498267.1:n.*89-196A>G
ENST00000652485.1:c.1866A>G	ENSP00000498973.1:p.Ile622Met
ENST00000378823.7:c.1833A>G	ENSP00000368100.4:p.Ile611Met
ENST00000423956.5:c.*19A>G	ENSP00000390971.1:n.*19A>G
ENST00000453394.5:c.1650A>G	ENSP00000400049.1:p.Ile550Met
ENST00000533482.5:c.*1459A>G	ENSP00000431225.1:n.*1459A>G
NM_005732.3:c.1833A>G	NP_005723.2:p.Ile611Met
NM_005732.4:c.1833A>G MANE Select	NP_005723.2:p.Ile611Met