Canonical Allele Identifier: CA2842557353
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435979_94435990del , CM000673.2:g.94435979_94435990del GRCh38
NC_000011.9:g.94169145_94169156del , CM000673.1:g.94169145_94169156del GRCh37
NC_000011.8:g.93808793_93808804del NCBI36
NG_007261.1:g.62885_62896del , LRG_85:g.62885_62896del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1927-91_1927-80del MANE Select ENSP00000325863.4:n.1927-91_1927-80del
ENST00000323929.7:c.1927-91_1927-80del ENSP00000325863.3:n.1927-91_1927-80del
ENST00000323977.7:c.1843-91_1843-80del ENSP00000326094.3:n.1843-91_1843-80del
ENST00000393241.8:c.1924-91_1924-80del ENSP00000376933.4:n.1924-91_1924-80del
ENST00000407439.7:c.1936-91_1936-80del ENSP00000385614.3:n.1936-91_1936-80del
NM_005590.3:c.1843-91_1843-80del NP_005581.2:n.1843-91_1843-80del
NM_005591.3:c.1927-91_1927-80del , LRG_85t1:c.1927-91_1927-80del NP_005582.1:n.1927-91_1927-80del
XM_005274008.2:c.1459-91_1459-80del XP_005274065.1:n.1459-91_1459-80del
XM_006718842.2:c.1924-91_1924-80del XP_006718905.1:n.1924-91_1924-80del
XM_011542837.1:c.1927-91_1927-80del XP_011541139.1:n.1927-91_1927-80del
XR_947828.1:n.2223-91_2223-80del
NM_001330347.1:c.1924-91_1924-80del NP_001317276.1:n.1924-91_1924-80del
XM_005274008.3:c.1459-91_1459-80del XP_005274065.1:n.1459-91_1459-80del
XM_006718842.3:c.1924-91_1924-80del XP_006718905.1:n.1924-91_1924-80del
XM_011542837.2:c.1927-91_1927-80del XP_011541139.1:n.1927-91_1927-80del
XM_017017772.1:c.1927-91_1927-80del XP_016873261.1:n.1927-91_1927-80del
XR_947828.2:n.2223-91_2223-80del
NM_001330347.2:c.1924-91_1924-80del NP_001317276.1:n.1924-91_1924-80del
NM_005590.4:c.1843-91_1843-80del NP_005581.2:n.1843-91_1843-80del
NM_005591.4:c.1927-91_1927-80del MANE Select NP_005582.1:n.1927-91_1927-80del