Canonical Allele Identifier: CA941028631
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1946351315

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94459340_94459389dup , CM000673.2:g.94459340_94459389dup GRCh38
NC_000011.9:g.94192506_94192555dup , CM000673.1:g.94192506_94192555dup GRCh37
NC_000011.8:g.93832154_93832203dup NCBI36
NG_007261.1:g.39487_39536dup , LRG_85:g.39487_39536dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1500+20_1500+69dup MANE Select ENSP00000325863.4:n.1500+20_1500+69dup
ENST00000323929.7:c.1500+20_1500+69dup ENSP00000325863.3:n.1500+20_1500+69dup
ENST00000323977.7:c.1500+20_1500+69dup ENSP00000326094.3:n.1500+20_1500+69dup
ENST00000393241.8:c.1500+20_1500+69dup ENSP00000376933.4:n.1500+20_1500+69dup
ENST00000407439.7:c.1509+20_1509+69dup ENSP00000385614.3:n.1509+20_1509+69dup
NM_005590.3:c.1500+20_1500+69dup NP_005581.2:n.1500+20_1500+69dup
NM_005591.3:c.1500+20_1500+69dup , LRG_85t1:c.1500+20_1500+69dup NP_005582.1:n.1500+20_1500+69dup
XM_005274008.2:c.1032+20_1032+69dup XP_005274065.1:n.1032+20_1032+69dup
XM_006718842.2:c.1500+20_1500+69dup XP_006718905.1:n.1500+20_1500+69dup
XM_011542837.1:c.1500+20_1500+69dup XP_011541139.1:n.1500+20_1500+69dup
XR_947828.1:n.1796+20_1796+69dup
NM_001330347.1:c.1500+20_1500+69dup NP_001317276.1:n.1500+20_1500+69dup
XM_005274008.3:c.1032+20_1032+69dup XP_005274065.1:n.1032+20_1032+69dup
XM_006718842.3:c.1500+20_1500+69dup XP_006718905.1:n.1500+20_1500+69dup
XM_011542837.2:c.1500+20_1500+69dup XP_011541139.1:n.1500+20_1500+69dup
XM_017017772.1:c.1500+20_1500+69dup XP_016873261.1:n.1500+20_1500+69dup
XR_947828.2:n.1796+20_1796+69dup
NM_001330347.2:c.1500+20_1500+69dup NP_001317276.1:n.1500+20_1500+69dup
NM_005590.4:c.1500+20_1500+69dup NP_005581.2:n.1500+20_1500+69dup
NM_005591.4:c.1500+20_1500+69dup MANE Select NP_005582.1:n.1500+20_1500+69dup