Canonical Allele Identifier: CA600838857
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1258484680

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94446026_94446037del , CM000673.2:g.94446026_94446037del GRCh38
NC_000011.9:g.94179192_94179203del , CM000673.1:g.94179192_94179203del GRCh37
NC_000011.8:g.93818840_93818851del NCBI36
NG_007261.1:g.52838_52849del , LRG_85:g.52838_52849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1784-144_1784-133del MANE Select ENSP00000325863.4:n.1784-144_1784-133del
ENST00000323929.7:c.1784-144_1784-133del ENSP00000325863.3:n.1784-144_1784-133del
ENST00000323977.7:c.1783+1182_1783+1193del ENSP00000326094.3:n.1783+1182_1783+1193del
ENST00000393241.8:c.1784-147_1784-136del ENSP00000376933.4:n.1784-147_1784-136del
ENST00000407439.7:c.1793-144_1793-133del ENSP00000385614.3:n.1793-144_1793-133del
ENST00000535120.1:n.83-147_83-136del
NM_005590.3:c.1783+1182_1783+1193del NP_005581.2:n.1783+1182_1783+1193del
NM_005591.3:c.1784-144_1784-133del , LRG_85t1:c.1784-144_1784-133del NP_005582.1:n.1784-144_1784-133del
XM_005274008.2:c.1316-144_1316-133del XP_005274065.1:n.1316-144_1316-133del
XM_006718842.2:c.1784-147_1784-136del XP_006718905.1:n.1784-147_1784-136del
XM_011542837.1:c.1784-144_1784-133del XP_011541139.1:n.1784-144_1784-133del
XR_947828.1:n.2080-144_2080-133del
NM_001330347.1:c.1784-147_1784-136del NP_001317276.1:n.1784-147_1784-136del
XM_005274008.3:c.1316-144_1316-133del XP_005274065.1:n.1316-144_1316-133del
XM_006718842.3:c.1784-147_1784-136del XP_006718905.1:n.1784-147_1784-136del
XM_011542837.2:c.1784-144_1784-133del XP_011541139.1:n.1784-144_1784-133del
XM_017017772.1:c.1784-144_1784-133del XP_016873261.1:n.1784-144_1784-133del
XR_947828.2:n.2080-144_2080-133del
NM_001330347.2:c.1784-147_1784-136del NP_001317276.1:n.1784-147_1784-136del
NM_005590.4:c.1783+1182_1783+1193del NP_005581.2:n.1783+1182_1783+1193del
NM_005591.4:c.1784-144_1784-133del MANE Select NP_005582.1:n.1784-144_1784-133del