Canonical Allele Identifier: CA1992442474
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94446008A= , CM000673.2:g.94446008A= GRCh38
NC_000011.9:g.94179174A= , CM000673.1:g.94179174A= GRCh37
NC_000011.8:g.93818822A= NCBI36
NG_007261.1:g.52867T= , LRG_85:g.52867T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1784-115T= MANE Select ENSP00000325863.4:n.1784-115T=
ENST00000323929.7:c.1784-115T= ENSP00000325863.3:n.1784-115T=
ENST00000323977.7:c.1783+1211T= ENSP00000326094.3:n.1783+1211T=
ENST00000393241.8:c.1784-118T= ENSP00000376933.4:n.1784-118T=
ENST00000407439.7:c.1793-115T= ENSP00000385614.3:n.1793-115T=
ENST00000535120.1:n.83-118T=
NM_005590.3:c.1783+1211T= NP_005581.2:n.1783+1211T=
NM_005591.3:c.1784-115T= , LRG_85t1:c.1784-115T= NP_005582.1:n.1784-115T=
XM_005274008.2:c.1316-115T= XP_005274065.1:n.1316-115T=
XM_006718842.2:c.1784-118T= XP_006718905.1:n.1784-118T=
XM_011542837.1:c.1784-115T= XP_011541139.1:n.1784-115T=
XR_947828.1:n.2080-115T=
NM_001330347.1:c.1784-118T= NP_001317276.1:n.1784-118T=
XM_005274008.3:c.1316-115T= XP_005274065.1:n.1316-115T=
XM_006718842.3:c.1784-118T= XP_006718905.1:n.1784-118T=
XM_011542837.2:c.1784-115T= XP_011541139.1:n.1784-115T=
XM_017017772.1:c.1784-115T= XP_016873261.1:n.1784-115T=
XR_947828.2:n.2080-115T=
NM_001330347.2:c.1784-118T= NP_001317276.1:n.1784-118T=
NM_005590.4:c.1783+1211T= NP_005581.2:n.1783+1211T=
NM_005591.4:c.1784-115T= MANE Select NP_005582.1:n.1784-115T=