Canonical Allele Identifier: CA682016125
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1231966811

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94436048_94436051del , CM000673.2:g.94436048_94436051del GRCh38
NC_000011.9:g.94169214_94169217del , CM000673.1:g.94169214_94169217del GRCh37
NC_000011.8:g.93808862_93808865del NCBI36
NG_007261.1:g.62826_62829del , LRG_85:g.62826_62829del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1927-150_1927-147del MANE Select ENSP00000325863.4:n.1927-150_1927-147del
ENST00000323929.7:c.1927-150_1927-147del ENSP00000325863.3:n.1927-150_1927-147del
ENST00000323977.7:c.1843-150_1843-147del ENSP00000326094.3:n.1843-150_1843-147del
ENST00000393241.8:c.1924-150_1924-147del ENSP00000376933.4:n.1924-150_1924-147del
ENST00000407439.7:c.1936-150_1936-147del ENSP00000385614.3:n.1936-150_1936-147del
NM_005590.3:c.1843-150_1843-147del NP_005581.2:n.1843-150_1843-147del
NM_005591.3:c.1927-150_1927-147del , LRG_85t1:c.1927-150_1927-147del NP_005582.1:n.1927-150_1927-147del
XM_005274008.2:c.1459-150_1459-147del XP_005274065.1:n.1459-150_1459-147del
XM_006718842.2:c.1924-150_1924-147del XP_006718905.1:n.1924-150_1924-147del
XM_011542837.1:c.1927-150_1927-147del XP_011541139.1:n.1927-150_1927-147del
XR_947828.1:n.2223-150_2223-147del
NM_001330347.1:c.1924-150_1924-147del NP_001317276.1:n.1924-150_1924-147del
XM_005274008.3:c.1459-150_1459-147del XP_005274065.1:n.1459-150_1459-147del
XM_006718842.3:c.1924-150_1924-147del XP_006718905.1:n.1924-150_1924-147del
XM_011542837.2:c.1927-150_1927-147del XP_011541139.1:n.1927-150_1927-147del
XM_017017772.1:c.1927-150_1927-147del XP_016873261.1:n.1927-150_1927-147del
XR_947828.2:n.2223-150_2223-147del
NM_001330347.2:c.1924-150_1924-147del NP_001317276.1:n.1924-150_1924-147del
NM_005590.4:c.1843-150_1843-147del NP_005581.2:n.1843-150_1843-147del
NM_005591.4:c.1927-150_1927-147del MANE Select NP_005582.1:n.1927-150_1927-147del