Canonical Allele Identifier: CA2793218393
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94436014_94436015insCCCAAACACACCCAACACA , CM000673.2:g.94436014_94436015insCCCAAACACACCCAACACA GRCh38
NC_000011.9:g.94169180_94169181insCCCAAACACACCCAACACA , CM000673.1:g.94169180_94169181insCCCAAACACACCCAACACA GRCh37
NC_000011.8:g.93808828_93808829insCCCAAACACACCCAACACA NCBI36
NG_007261.1:g.62861_62862insGTGTTGGGTGTGTTTGGGT , LRG_85:g.62861_62862insGTGTTGGGTGTGTTTGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT MANE Select ENSP00000325863.4:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT
ENST00000323929.7:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT ENSP00000325863.3:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT
ENST00000323977.7:c.1843-115_1843-114insGTGTTGGGTGTGTTTGGGT ENSP00000326094.3:n.1843-115_1843-114insGTGTTGGGTGTGTTTGGGT
ENST00000393241.8:c.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT ENSP00000376933.4:n.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT
ENST00000407439.7:c.1936-115_1936-114insGTGTTGGGTGTGTTTGGGT ENSP00000385614.3:n.1936-115_1936-114insGTGTTGGGTGTGTTTGGGT
NM_005590.3:c.1843-115_1843-114insGTGTTGGGTGTGTTTGGGT NP_005581.2:n.1843-115_1843-114insGTGTTGGGTGTGTTTGGGT
NM_005591.3:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT , LRG_85t1:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT NP_005582.1:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT
XM_005274008.2:c.1459-115_1459-114insGTGTTGGGTGTGTTTGGGT XP_005274065.1:n.1459-115_1459-114insGTGTTGGGTGTGTTTGGGT
XM_006718842.2:c.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT XP_006718905.1:n.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT
XM_011542837.1:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT XP_011541139.1:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT
XR_947828.1:n.2223-115_2223-114insGTGTTGGGTGTGTTTGGGT
NM_001330347.1:c.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT NP_001317276.1:n.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT
XM_005274008.3:c.1459-115_1459-114insGTGTTGGGTGTGTTTGGGT XP_005274065.1:n.1459-115_1459-114insGTGTTGGGTGTGTTTGGGT
XM_006718842.3:c.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT XP_006718905.1:n.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT
XM_011542837.2:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT XP_011541139.1:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT
XM_017017772.1:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT XP_016873261.1:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT
XR_947828.2:n.2223-115_2223-114insGTGTTGGGTGTGTTTGGGT
NM_001330347.2:c.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT NP_001317276.1:n.1924-115_1924-114insGTGTTGGGTGTGTTTGGGT
NM_005590.4:c.1843-115_1843-114insGTGTTGGGTGTGTTTGGGT NP_005581.2:n.1843-115_1843-114insGTGTTGGGTGTGTTTGGGT
NM_005591.4:c.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT MANE Select NP_005582.1:n.1927-115_1927-114insGTGTTGGGTGTGTTTGGGT