Canonical Allele Identifier: CA1583246285
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132604857A= , CM000667.2:g.132604857A= GRCh38
NC_000005.9:g.131940549A= , CM000667.1:g.131940549A= GRCh37
NC_000005.8:g.131968448A= NCBI36
NG_021151.1:g.52934A=
NG_021151.2:g.52881A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.2576A= MANE Select ENSP00000368100.4:p.Gln859=
ENST00000638452.2:c.2279A= ENSP00000492349.2:p.Gln760=
ENST00000638504.1:n.2184A=
ENST00000638568.2:c.2279A= ENSP00000491158.2:p.Gln760=
ENST00000639899.1:n.3095A=
ENST00000640655.2:c.2279A= ENSP00000491596.2:p.Gln760=
ENST00000651160.1:c.*720A= ENSP00000498829.1:n.*720A=
ENST00000651723.1:c.*2659A= ENSP00000498237.1:n.*2659A=
ENST00000652016.1:c.*793A= ENSP00000498267.1:n.*793A=
ENST00000652485.1:c.2609A= ENSP00000498973.1:p.Gln870=
ENST00000378823.7:c.2576A= ENSP00000368100.4:p.Gln859=
ENST00000423956.5:c.*762A= ENSP00000390971.1:n.*762A=
ENST00000533482.5:c.*2202A= ENSP00000431225.1:n.*2202A=
NM_005732.3:c.2576A= NP_005723.2:p.Gln859=
NM_005732.4:c.2576A= MANE Select NP_005723.2:p.Gln859=