Canonical Allele Identifier: CA360959734

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131944859C>A (hg19) ; chr5:g.132609167C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609167C>A , CM000667.2:g.132609167C>A	GRCh38
NC_000005.9:g.131944859C>A , CM000667.1:g.131944859C>A	GRCh37
NC_000005.8:g.131972758C>A	NCBI36
NG_021151.1:g.57244C>A
NG_021151.2:g.57191C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2880C>A MANE Select	ENSP00000368100.4:p.Asp960Glu
ENST00000638452.2:c.2583C>A	ENSP00000492349.2:p.Asp861Glu
ENST00000638504.1:n.2488C>A
ENST00000638568.2:c.2583C>A	ENSP00000491158.2:p.Asp861Glu
ENST00000639899.1:n.3399C>A
ENST00000640655.2:c.2583C>A	ENSP00000491596.2:p.Asp861Glu
ENST00000651160.1:c.*1024C>A	ENSP00000498829.1:n.*1024C>A
ENST00000651723.1:c.*2963C>A	ENSP00000498237.1:n.*2963C>A
ENST00000378823.7:c.2880C>A	ENSP00000368100.4:p.Asp960Glu
ENST00000423956.5:c.*1066C>A	ENSP00000390971.1:n.*1066C>A
ENST00000533482.5:c.*2506C>A	ENSP00000431225.1:n.*2506C>A
NM_005732.3:c.2880C>A	NP_005723.2:p.Asp960Glu
NM_005732.4:c.2880C>A MANE Select	NP_005723.2:p.Asp960Glu