Canonical Allele Identifier: CA1992436765
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94478795T= , CM000673.2:g.94478795T= GRCh38
NC_000011.9:g.94211961T= , CM000673.1:g.94211961T= GRCh37
NC_000011.8:g.93851609T= NCBI36
NG_007261.1:g.20080A= , LRG_85:g.20080A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.484A= MANE Select ENSP00000325863.4:p.Ile162=
ENST00000323929.7:c.484A= ENSP00000325863.3:p.Ile162=
ENST00000323977.7:c.484A= ENSP00000326094.3:p.Ile162=
ENST00000393241.8:c.484A= ENSP00000376933.4:p.Ile162=
ENST00000407439.7:c.493A= ENSP00000385614.3:p.Ile165=
ENST00000540013.5:c.484A= ENSP00000440986.1:p.Ile162=
ENST00000541157.5:n.560A=
NM_005590.3:c.484A= NP_005581.2:p.Ile162=
NM_005591.3:c.484A= , LRG_85t1:c.484A= NP_005582.1:p.Ile162=
XM_005274008.2:c.16A= XP_005274065.1:p.Ile6=
XM_006718842.2:c.484A= XP_006718905.1:p.Ile162=
XM_011542837.1:c.484A= XP_011541139.1:p.Ile162=
XR_947828.1:n.780A=
NM_001330347.1:c.484A= NP_001317276.1:p.Ile162=
XM_005274008.3:c.16A= XP_005274065.1:p.Ile6=
XM_006718842.3:c.484A= XP_006718905.1:p.Ile162=
XM_011542837.2:c.484A= XP_011541139.1:p.Ile162=
XM_017017772.1:c.484A= XP_016873261.1:p.Ile162=
XR_947828.2:n.780A=
NM_001330347.2:c.484A= NP_001317276.1:p.Ile162=
NM_005590.4:c.484A= NP_005581.2:p.Ile162=
NM_005591.4:c.484A= MANE Select NP_005582.1:p.Ile162=