Canonical Allele Identifier: CA645559199
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132595767_132595768del , CM000667.2:g.132595767_132595768del GRCh38
NC_000005.9:g.131931459_131931460del , CM000667.1:g.131931459_131931460del GRCh37
NC_000005.8:g.131959358_131959359del NCBI36
NG_021151.1:g.43844_43845del
NG_021151.2:g.43791_43792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.2164_2165del MANE Select ENSP00000368100.4:p.Lys722GlyfsTer5
ENST00000638452.2:c.1867_1868del ENSP00000492349.2:p.Lys623GlyfsTer5
ENST00000638504.1:n.1772_1773del
ENST00000638568.2:c.1867_1868del ENSP00000491158.2:p.Lys623GlyfsTer5
ENST00000639899.1:n.2683_2684del
ENST00000640655.2:c.1867_1868del ENSP00000491596.2:p.Lys623GlyfsTer5
ENST00000651160.1:c.*308_*309del ENSP00000498829.1:n.*308_*309del
ENST00000651658.1:n.2707_2708del
ENST00000651723.1:c.*2247_*2248del ENSP00000498237.1:n.*2247_*2248del
ENST00000652016.1:c.*381_*382del ENSP00000498267.1:n.*381_*382del
ENST00000652485.1:c.2197_2198del ENSP00000498973.1:p.Lys733GlyfsTer5
ENST00000378823.7:c.2164_2165del ENSP00000368100.4:p.Lys722GlyfsTer5
ENST00000423956.5:c.*350_*351del ENSP00000390971.1:n.*350_*351del
ENST00000453394.5:c.1981_1982del
ENST00000496204.1:n.247_248del
ENST00000533482.5:c.*1790_*1791del ENSP00000431225.1:n.*1790_*1791del
NM_005732.3:c.2164_2165del NP_005723.2:p.Lys722GlyfsTer5
NM_005732.4:c.2164_2165del MANE Select NP_005723.2:p.Lys722GlyfsTer5