Canonical Allele Identifier: CA2578402706

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604781A>G , CM000667.2:g.132604781A>G	GRCh38
NC_000005.9:g.131940473A>G , CM000667.1:g.131940473A>G	GRCh37
NC_000005.8:g.131968372A>G	NCBI36
NG_021151.1:g.52858A>G
NG_021151.2:g.52805A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2525-25A>G MANE Select	ENSP00000368100.4:n.2525-25A>G
ENST00000638452.2:c.2228-25A>G	ENSP00000492349.2:n.2228-25A>G
ENST00000638504.1:n.2133-25A>G
ENST00000638568.2:c.2228-25A>G	ENSP00000491158.2:n.2228-25A>G
ENST00000639899.1:n.3044-25A>G
ENST00000640655.2:c.2228-25A>G	ENSP00000491596.2:n.2228-25A>G
ENST00000651160.1:c.*669-25A>G	ENSP00000498829.1:n.*669-25A>G
ENST00000651723.1:c.*2608-25A>G	ENSP00000498237.1:n.*2608-25A>G
ENST00000652016.1:c.*742-25A>G	ENSP00000498267.1:n.*742-25A>G
ENST00000652485.1:c.2558-25A>G	ENSP00000498973.1:n.2558-25A>G
ENST00000378823.7:c.2525-25A>G	ENSP00000368100.4:n.2525-25A>G
ENST00000423956.5:c.*711-25A>G	ENSP00000390971.1:n.*711-25A>G
ENST00000533482.5:c.*2151-25A>G	ENSP00000431225.1:n.*2151-25A>G
NM_005732.3:c.2525-25A>G	NP_005723.2:n.2525-25A>G
NM_005732.4:c.2525-25A>G MANE Select	NP_005723.2:n.2525-25A>G