Canonical Allele Identifier: CA600852535
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1224148872

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94436014dup , CM000673.2:g.94436014dup GRCh38
NC_000011.9:g.94169180dup , CM000673.1:g.94169180dup GRCh37
NC_000011.8:g.93808828dup NCBI36
NG_007261.1:g.62866dup , LRG_85:g.62866dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1927-110dup MANE Select ENSP00000325863.4:n.1927-110dup
ENST00000323929.7:c.1927-110dup ENSP00000325863.3:n.1927-110dup
ENST00000323977.7:c.1843-110dup ENSP00000326094.3:n.1843-110dup
ENST00000393241.8:c.1924-110dup ENSP00000376933.4:n.1924-110dup
ENST00000407439.7:c.1936-110dup ENSP00000385614.3:n.1936-110dup
NM_005590.3:c.1843-110dup NP_005581.2:n.1843-110dup
NM_005591.3:c.1927-110dup , LRG_85t1:c.1927-110dup NP_005582.1:n.1927-110dup
XM_005274008.2:c.1459-110dup XP_005274065.1:n.1459-110dup
XM_006718842.2:c.1924-110dup XP_006718905.1:n.1924-110dup
XM_011542837.1:c.1927-110dup XP_011541139.1:n.1927-110dup
XR_947828.1:n.2223-110dup
NM_001330347.1:c.1924-110dup NP_001317276.1:n.1924-110dup
XM_005274008.3:c.1459-110dup XP_005274065.1:n.1459-110dup
XM_006718842.3:c.1924-110dup XP_006718905.1:n.1924-110dup
XM_011542837.2:c.1927-110dup XP_011541139.1:n.1927-110dup
XM_017017772.1:c.1927-110dup XP_016873261.1:n.1927-110dup
XR_947828.2:n.2223-110dup
NM_001330347.2:c.1924-110dup NP_001317276.1:n.1924-110dup
NM_005590.4:c.1843-110dup NP_005581.2:n.1843-110dup
NM_005591.4:c.1927-110dup MANE Select NP_005582.1:n.1927-110dup