Canonical Allele Identifier: CA2724798396
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs2135001880

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94464329_94464330insTC , CM000673.2:g.94464329_94464330insTC GRCh38
NC_000011.9:g.94197495_94197496insTC , CM000673.1:g.94197495_94197496insTC GRCh37
NC_000011.8:g.93837143_93837144insTC NCBI36
NG_007261.1:g.34545_34546insGA , LRG_85:g.34545_34546insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1099-91_1099-90insGA MANE Select ENSP00000325863.4:n.1099-91_1099-90insGA
ENST00000323929.7:c.1099-91_1099-90insGA ENSP00000325863.3:n.1099-91_1099-90insGA
ENST00000323977.7:c.1099-91_1099-90insGA ENSP00000326094.3:n.1099-91_1099-90insGA
ENST00000393241.8:c.1099-91_1099-90insGA ENSP00000376933.4:n.1099-91_1099-90insGA
ENST00000407439.7:c.1108-91_1108-90insGA ENSP00000385614.3:n.1108-91_1108-90insGA
NM_005590.3:c.1099-91_1099-90insGA NP_005581.2:n.1099-91_1099-90insGA
NM_005591.3:c.1099-91_1099-90insGA , LRG_85t1:c.1099-91_1099-90insGA NP_005582.1:n.1099-91_1099-90insGA
XM_005274008.2:c.631-91_631-90insGA XP_005274065.1:n.631-91_631-90insGA
XM_006718842.2:c.1099-91_1099-90insGA XP_006718905.1:n.1099-91_1099-90insGA
XM_011542837.1:c.1099-91_1099-90insGA XP_011541139.1:n.1099-91_1099-90insGA
XR_947828.1:n.1395-91_1395-90insGA
NM_001330347.1:c.1099-91_1099-90insGA NP_001317276.1:n.1099-91_1099-90insGA
XM_005274008.3:c.631-91_631-90insGA XP_005274065.1:n.631-91_631-90insGA
XM_006718842.3:c.1099-91_1099-90insGA XP_006718905.1:n.1099-91_1099-90insGA
XM_011542837.2:c.1099-91_1099-90insGA XP_011541139.1:n.1099-91_1099-90insGA
XM_017017772.1:c.1099-91_1099-90insGA XP_016873261.1:n.1099-91_1099-90insGA
XR_947828.2:n.1395-91_1395-90insGA
NM_001330347.2:c.1099-91_1099-90insGA NP_001317276.1:n.1099-91_1099-90insGA
NM_005590.4:c.1099-91_1099-90insGA NP_005581.2:n.1099-91_1099-90insGA
NM_005591.4:c.1099-91_1099-90insGA MANE Select NP_005582.1:n.1099-91_1099-90insGA