Canonical Allele Identifier: CA1992453997
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94488222_94488225delinsACCT , CM000673.2:g.94488222_94488225delinsACCT GRCh38
NC_000011.9:g.94221388_94221391delinsACCT , CM000673.1:g.94221388_94221391delinsACCT GRCh37
NC_000011.8:g.93861036_93861039delinsACCT NCBI36
NG_007261.1:g.10650_10653delinsAGGT , LRG_85:g.10650_10653delinsAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.154-2141_154-2138delinsAGGT MANE Select ENSP00000325863.4:n.154-2141_154-2138deli...
ENST00000323929.7:c.154-2141_154-2138delinsAGGT ENSP00000325863.3:n.154-2141_154-2138deli...
ENST00000323977.7:c.154-2141_154-2138delinsAGGT ENSP00000326094.3:n.154-2141_154-2138deli...
ENST00000393241.8:c.154-2141_154-2138delinsAGGT ENSP00000376933.4:n.154-2141_154-2138deli...
ENST00000407439.7:c.163-2141_163-2138delinsAGGT ENSP00000385614.3:n.163-2141_163-2138deli...
ENST00000536144.1:n.389-2141_389-2138delinsAGGT
ENST00000536754.5:c.154-2141_154-2138delinsAGGT ENSP00000439511.1:n.154-2141_154-2138deli...
ENST00000538923.1:c.154-2141_154-2138delinsAGGT ENSP00000442809.1:n.154-2141_154-2138deli...
ENST00000540013.5:c.154-2141_154-2138delinsAGGT ENSP00000440986.1:n.154-2141_154-2138deli...
ENST00000541157.5:n.318-2141_318-2138delinsAGGT
NM_005590.3:c.154-2141_154-2138delinsAGGT NP_005581.2:n.154-2141_154-2138delinsAGGT...
NM_005591.3:c.154-2141_154-2138delinsAGGT , LRG_85t1:c.154-2141_154-2138delinsAGGT NP_005582.1:n.154-2141_154-2138delinsAGGT...
XM_006718842.2:c.154-2141_154-2138delinsAGGT XP_006718905.1:n.154-2141_154-2138delinsA...
XM_011542837.1:c.154-2141_154-2138delinsAGGT XP_011541139.1:n.154-2141_154-2138delinsA...
XR_947828.1:n.450-2141_450-2138delinsAGGT
NM_001330347.1:c.154-2141_154-2138delinsAGGT NP_001317276.1:n.154-2141_154-2138delinsA...
XM_005274008.3:c.-311-2141_-311-2138delinsAGGT XP_005274065.1:n.-311-2141_-311-2138delin...
XM_006718842.3:c.154-2141_154-2138delinsAGGT XP_006718905.1:n.154-2141_154-2138delinsA...
XM_011542837.2:c.154-2141_154-2138delinsAGGT XP_011541139.1:n.154-2141_154-2138delinsA...
XM_017017772.1:c.154-2141_154-2138delinsAGGT XP_016873261.1:n.154-2141_154-2138delinsA...
XR_947828.2:n.450-2141_450-2138delinsAGGT
NM_001330347.2:c.154-2141_154-2138delinsAGGT NP_001317276.1:n.154-2141_154-2138delinsA...
NM_005590.4:c.154-2141_154-2138delinsAGGT NP_005581.2:n.154-2141_154-2138delinsAGGT...
NM_005591.4:c.154-2141_154-2138delinsAGGT MANE Select NP_005582.1:n.154-2141_154-2138delinsAGGT...