Canonical Allele Identifier: CA1992453857
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94488082_94488083delinsAG , CM000673.2:g.94488082_94488083delinsAG GRCh38
NC_000011.9:g.94221248_94221249delinsAG , CM000673.1:g.94221248_94221249delinsAG GRCh37
NC_000011.8:g.93860896_93860897delinsAG NCBI36
NG_007261.1:g.10792_10793delinsCT , LRG_85:g.10792_10793delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.154-1999_154-1998delinsCT MANE Select ENSP00000325863.4:n.154-1999_154-1998delinsCT
ENST00000323929.7:c.154-1999_154-1998delinsCT ENSP00000325863.3:n.154-1999_154-1998delinsCT
ENST00000323977.7:c.154-1999_154-1998delinsCT ENSP00000326094.3:n.154-1999_154-1998delinsCT
ENST00000393241.8:c.154-1999_154-1998delinsCT ENSP00000376933.4:n.154-1999_154-1998delinsCT
ENST00000407439.7:c.163-1999_163-1998delinsCT ENSP00000385614.3:n.163-1999_163-1998delinsCT
ENST00000536144.1:n.389-1999_389-1998delinsCT
ENST00000536754.5:c.154-1999_154-1998delinsCT ENSP00000439511.1:n.154-1999_154-1998delinsCT
ENST00000538923.1:c.154-1999_154-1998delinsCT ENSP00000442809.1:n.154-1999_154-1998delinsCT
ENST00000540013.5:c.154-1999_154-1998delinsCT ENSP00000440986.1:n.154-1999_154-1998delinsCT
ENST00000541157.5:n.318-1999_318-1998delinsCT
NM_005590.3:c.154-1999_154-1998delinsCT NP_005581.2:n.154-1999_154-1998delinsCT
NM_005591.3:c.154-1999_154-1998delinsCT , LRG_85t1:c.154-1999_154-1998delinsCT NP_005582.1:n.154-1999_154-1998delinsCT
XM_006718842.2:c.154-1999_154-1998delinsCT XP_006718905.1:n.154-1999_154-1998delinsCT
XM_011542837.1:c.154-1999_154-1998delinsCT XP_011541139.1:n.154-1999_154-1998delinsCT
XR_947828.1:n.450-1999_450-1998delinsCT
NM_001330347.1:c.154-1999_154-1998delinsCT NP_001317276.1:n.154-1999_154-1998delinsCT
XM_005274008.3:c.-311-1999_-311-1998delinsCT XP_005274065.1:n.-311-1999_-311-1998delinsCT
XM_006718842.3:c.154-1999_154-1998delinsCT XP_006718905.1:n.154-1999_154-1998delinsCT
XM_011542837.2:c.154-1999_154-1998delinsCT XP_011541139.1:n.154-1999_154-1998delinsCT
XM_017017772.1:c.154-1999_154-1998delinsCT XP_016873261.1:n.154-1999_154-1998delinsCT
XR_947828.2:n.450-1999_450-1998delinsCT
NM_001330347.2:c.154-1999_154-1998delinsCT NP_001317276.1:n.154-1999_154-1998delinsCT
NM_005590.4:c.154-1999_154-1998delinsCT NP_005581.2:n.154-1999_154-1998delinsCT
NM_005591.4:c.154-1999_154-1998delinsCT MANE Select NP_005582.1:n.154-1999_154-1998delinsCT