Canonical Allele Identifier: CA2574952535
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445921del , CM000673.2:g.94445921del GRCh38
NC_000011.9:g.94179087del , CM000673.1:g.94179087del GRCh37
NC_000011.8:g.93818735del NCBI36
NG_007261.1:g.52954del , LRG_85:g.52954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1784-28del MANE Select ENSP00000325863.4:n.1784-28del
ENST00000323929.7:c.1784-28del ENSP00000325863.3:n.1784-28del
ENST00000323977.7:c.1783+1298del ENSP00000326094.3:n.1783+1298del
ENST00000393241.8:c.1784-31del ENSP00000376933.4:n.1784-31del
ENST00000407439.7:c.1793-28del ENSP00000385614.3:n.1793-28del
ENST00000535120.1:n.83-31del
NM_005590.3:c.1783+1298del NP_005581.2:n.1783+1298del
NM_005591.3:c.1784-28del , LRG_85t1:c.1784-28del NP_005582.1:n.1784-28del
XM_005274008.2:c.1316-28del XP_005274065.1:n.1316-28del
XM_006718842.2:c.1784-31del XP_006718905.1:n.1784-31del
XM_011542837.1:c.1784-28del XP_011541139.1:n.1784-28del
XR_947828.1:n.2080-28del
NM_001330347.1:c.1784-31del NP_001317276.1:n.1784-31del
XM_005274008.3:c.1316-28del XP_005274065.1:n.1316-28del
XM_006718842.3:c.1784-31del XP_006718905.1:n.1784-31del
XM_011542837.2:c.1784-28del XP_011541139.1:n.1784-28del
XM_017017772.1:c.1784-28del XP_016873261.1:n.1784-28del
XR_947828.2:n.2080-28del
NM_001330347.2:c.1784-31del NP_001317276.1:n.1784-31del
NM_005590.4:c.1783+1298del NP_005581.2:n.1783+1298del
NM_005591.4:c.1784-28del MANE Select NP_005582.1:n.1784-28del