Canonical Allele Identifier: CA1992438905
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94479735C= , CM000673.2:g.94479735C= GRCh38
NC_000011.9:g.94212901C= , CM000673.1:g.94212901C= GRCh37
NC_000011.8:g.93852549C= NCBI36
NG_007261.1:g.19140G= , LRG_85:g.19140G=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.341G= MANE Select ENSP00000325863.4:p.Gly114=
ENST00000323929.7:c.341G= ENSP00000325863.3:p.Gly114=
ENST00000323977.7:c.341G= ENSP00000326094.3:p.Gly114=
ENST00000393241.8:c.341G= ENSP00000376933.4:p.Gly114=
ENST00000407439.7:c.350G= ENSP00000385614.3:p.Gly117=
ENST00000536754.5:c.341G= ENSP00000439511.1:p.Gly114=
ENST00000540013.5:c.341G= ENSP00000440986.1:p.Gly114=
ENST00000541157.5:n.479-859G=
NM_005590.3:c.341G= NP_005581.2:p.Gly114=
NM_005591.3:c.341G= , LRG_85t1:c.341G= NP_005582.1:p.Gly114=
XM_005274008.2:c.-128G= XP_005274065.1:n.-128G=
XM_006718842.2:c.341G= XP_006718905.1:p.Gly114=
XM_011542837.1:c.341G= XP_011541139.1:p.Gly114=
XR_947828.1:n.637G=
NM_001330347.1:c.341G= NP_001317276.1:p.Gly114=
XM_005274008.3:c.-128G= XP_005274065.1:n.-128G=
XM_006718842.3:c.341G= XP_006718905.1:p.Gly114=
XM_011542837.2:c.341G= XP_011541139.1:p.Gly114=
XM_017017772.1:c.341G= XP_016873261.1:p.Gly114=
XR_947828.2:n.637G=
NM_001330347.2:c.341G= NP_001317276.1:p.Gly114=
NM_005590.4:c.341G= NP_005581.2:p.Gly114=
NM_005591.4:c.341G= MANE Select NP_005582.1:p.Gly114=