Canonical Allele Identifier: CA1992426134
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1945594972

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435870_94435872del , CM000673.2:g.94435870_94435872del GRCh38
NC_000011.9:g.94169036_94169038del , CM000673.1:g.94169036_94169038del GRCh37
NC_000011.8:g.93808684_93808686del NCBI36
NG_007261.1:g.63008_63010del , LRG_85:g.63008_63010del

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1959_1961del MANE Select ENSP00000325863.4:p.Glu653del
ENST00000323929.7:c.1959_1961del ENSP00000325863.3:p.Glu653del
ENST00000323977.7:c.1875_1877del ENSP00000326094.3:p.Glu625del
ENST00000393241.8:c.1956_1958del ENSP00000376933.4:p.Glu652del
ENST00000407439.7:c.1968_1970del ENSP00000385614.3:p.Glu656del
NM_005590.3:c.1875_1877del NP_005581.2:p.Glu625del
NM_005591.3:c.1959_1961del , LRG_85t1:c.1959_1961del NP_005582.1:p.Glu653del
XM_005274008.2:c.1491_1493del XP_005274065.1:p.Glu497del
XM_006718842.2:c.1956_1958del XP_006718905.1:p.Glu652del
XM_011542837.1:c.1959_1961del XP_011541139.1:p.Glu653del
XR_947828.1:n.2255_2257del
NM_001330347.1:c.1956_1958del NP_001317276.1:p.Glu652del
XM_005274008.3:c.1491_1493del XP_005274065.1:p.Glu497del
XM_006718842.3:c.1956_1958del XP_006718905.1:p.Glu652del
XM_011542837.2:c.1959_1961del XP_011541139.1:p.Glu653del
XM_017017772.1:c.1959_1961del XP_016873261.1:p.Glu653del
XR_947828.2:n.2255_2257del
NM_001330347.2:c.1956_1958del NP_001317276.1:p.Glu652del
NM_005590.4:c.1875_1877del NP_005581.2:p.Glu625del
NM_005591.4:c.1959_1961del MANE Select NP_005582.1:p.Glu653del