Canonical Allele Identifier: CA2578402715
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618001A>T , CM000667.2:g.132618001A>T GRCh38
NC_000005.9:g.131953693A>T , CM000667.1:g.131953693A>T GRCh37
NC_000005.8:g.131981592A>T NCBI36
NG_021151.1:g.66078A>T
NG_021151.2:g.66025A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.3165-69A>T MANE Select ENSP00000368100.4:n.3165-69A>T
ENST00000638452.2:c.2868-69A>T ENSP00000492349.2:n.2868-69A>T
ENST00000638504.1:n.2773-69A>T
ENST00000638568.2:c.2868-69A>T ENSP00000491158.2:n.2868-69A>T
ENST00000639899.1:n.3684-69A>T
ENST00000640655.2:c.2868-69A>T ENSP00000491596.2:n.2868-69A>T
ENST00000378823.7:c.3165-69A>T ENSP00000368100.4:n.3165-69A>T
ENST00000533482.5:c.*2791-69A>T ENSP00000431225.1:n.*2791-69A>T
NM_005732.3:c.3165-69A>T NP_005723.2:n.3165-69A>T
NM_005732.4:c.3165-69A>T MANE Select NP_005723.2:n.3165-69A>T