Canonical Allele Identifier: CA2615589141
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94463967_94463971del , CM000673.2:g.94463967_94463971del GRCh38
NC_000011.9:g.94197133_94197137del , CM000673.1:g.94197133_94197137del GRCh37
NC_000011.8:g.93836781_93836785del NCBI36
NG_007261.1:g.34908_34912del , LRG_85:g.34908_34912del

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1225+146_1225+150del MANE Select ENSP00000325863.4:n.1225+146_1225+150del
ENST00000323929.7:c.1225+146_1225+150del ENSP00000325863.3:n.1225+146_1225+150del
ENST00000323977.7:c.1225+146_1225+150del ENSP00000326094.3:n.1225+146_1225+150del
ENST00000393241.8:c.1225+146_1225+150del ENSP00000376933.4:n.1225+146_1225+150del
ENST00000407439.7:c.1234+146_1234+150del ENSP00000385614.3:n.1234+146_1234+150del
NM_005590.3:c.1225+146_1225+150del NP_005581.2:n.1225+146_1225+150del
NM_005591.3:c.1225+146_1225+150del , LRG_85t1:c.1225+146_1225+150del NP_005582.1:n.1225+146_1225+150del
XM_005274008.2:c.757+146_757+150del XP_005274065.1:n.757+146_757+150del
XM_006718842.2:c.1225+146_1225+150del XP_006718905.1:n.1225+146_1225+150del
XM_011542837.1:c.1225+146_1225+150del XP_011541139.1:n.1225+146_1225+150del
XR_947828.1:n.1521+146_1521+150del
NM_001330347.1:c.1225+146_1225+150del NP_001317276.1:n.1225+146_1225+150del
XM_005274008.3:c.757+146_757+150del XP_005274065.1:n.757+146_757+150del
XM_006718842.3:c.1225+146_1225+150del XP_006718905.1:n.1225+146_1225+150del
XM_011542837.2:c.1225+146_1225+150del XP_011541139.1:n.1225+146_1225+150del
XM_017017772.1:c.1225+146_1225+150del XP_016873261.1:n.1225+146_1225+150del
XR_947828.2:n.1521+146_1521+150del
NM_001330347.2:c.1225+146_1225+150del NP_001317276.1:n.1225+146_1225+150del
NM_005590.4:c.1225+146_1225+150del NP_005581.2:n.1225+146_1225+150del
NM_005591.4:c.1225+146_1225+150del MANE Select NP_005582.1:n.1225+146_1225+150del