Canonical Allele Identifier: CA1583227139
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132579961G= , CM000667.2:g.132579961G= GRCh38
NC_000005.9:g.131915653G= , CM000667.1:g.131915653G= GRCh37
NC_000005.8:g.131943552G= NCBI36
NG_021151.1:g.28038G=
NG_021151.2:g.27985G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.651G= MANE Select ENSP00000368100.4:p.Lys217=
ENST00000638452.2:c.354G= ENSP00000492349.2:p.Lys118=
ENST00000638504.1:n.442+4033G=
ENST00000638568.2:c.354G= ENSP00000491158.2:p.Lys118=
ENST00000639899.1:n.1170G=
ENST00000640655.2:c.354G= ENSP00000491596.2:p.Lys118=
ENST00000651160.1:c.651G= ENSP00000498829.1:p.Lys217=
ENST00000651541.1:c.354G= ENSP00000498795.1:p.Lys118=
ENST00000651658.1:n.1078G=
ENST00000651723.1:c.*734G= ENSP00000498237.1:n.*734G=
ENST00000652016.1:c.651G= ENSP00000498267.1:p.Lys217=
ENST00000652485.1:c.651G= ENSP00000498973.1:p.Lys217=
ENST00000378823.7:c.651G= ENSP00000368100.4:p.Lys217=
ENST00000423956.5:c.651G= ENSP00000390971.1:p.Lys217=
ENST00000453394.5:c.651G= ENSP00000400049.1:p.Lys217=
ENST00000487596.1:n.217G=
ENST00000533482.5:c.*277G= ENSP00000431225.1:n.*277G=
NM_005732.3:c.651G= NP_005723.2:p.Lys217=
NM_005732.4:c.651G= MANE Select NP_005723.2:p.Lys217=