Canonical Allele Identifier: CA382366721
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445862G>C , CM000673.2:g.94445862G>C GRCh38
NC_000011.9:g.94179028G>C , CM000673.1:g.94179028G>C GRCh37
NC_000011.8:g.93818676G>C NCBI36
NG_007261.1:g.53013C>G , LRG_85:g.53013C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1815C>G MANE Select ENSP00000325863.4:p.Ser605Arg
ENST00000323929.7:c.1815C>G ENSP00000325863.3:p.Ser605Arg
ENST00000323977.7:c.1783+1357C>G ENSP00000326094.3:n.1783+1357C>G
ENST00000393241.8:c.1812C>G ENSP00000376933.4:p.Ser604Arg
ENST00000407439.7:c.1824C>G ENSP00000385614.3:p.Ser608Arg
ENST00000535120.1:n.111C>G
NM_005590.3:c.1783+1357C>G NP_005581.2:n.1783+1357C>G
NM_005591.3:c.1815C>G , LRG_85t1:c.1815C>G NP_005582.1:p.Ser605Arg
XM_005274008.2:c.1347C>G XP_005274065.1:p.Ser449Arg
XM_006718842.2:c.1812C>G XP_006718905.1:p.Ser604Arg
XM_011542837.1:c.1815C>G XP_011541139.1:p.Ser605Arg
XR_947828.1:n.2111C>G
NM_001330347.1:c.1812C>G NP_001317276.1:p.Ser604Arg
XM_005274008.3:c.1347C>G XP_005274065.1:p.Ser449Arg
XM_006718842.3:c.1812C>G XP_006718905.1:p.Ser604Arg
XM_011542837.2:c.1815C>G XP_011541139.1:p.Ser605Arg
XM_017017772.1:c.1815C>G XP_016873261.1:p.Ser605Arg
XR_947828.2:n.2111C>G
NM_001330347.2:c.1812C>G NP_001317276.1:p.Ser604Arg
NM_005590.4:c.1783+1357C>G NP_005581.2:n.1783+1357C>G
NM_005591.4:c.1815C>G MANE Select NP_005582.1:p.Ser605Arg