Canonical Allele Identifier: CA941023277
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1945930295

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94446327_94446328del , CM000673.2:g.94446327_94446328del GRCh38
NC_000011.9:g.94179493_94179494del , CM000673.1:g.94179493_94179494del GRCh37
NC_000011.8:g.93819141_93819142del NCBI36
NG_007261.1:g.52547_52548del , LRG_85:g.52547_52548del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1784-435_1784-434del MANE Select ENSP00000325863.4:n.1784-435_1784-434del
ENST00000323929.7:c.1784-435_1784-434del ENSP00000325863.3:n.1784-435_1784-434del
ENST00000323977.7:c.1783+891_1783+892del ENSP00000326094.3:n.1783+891_1783+892del
ENST00000393241.8:c.1784-438_1784-437del ENSP00000376933.4:n.1784-438_1784-437del
ENST00000407439.7:c.1793-435_1793-434del ENSP00000385614.3:n.1793-435_1793-434del
ENST00000535120.1:n.83-438_83-437del
NM_005590.3:c.1783+891_1783+892del NP_005581.2:n.1783+891_1783+892del
NM_005591.3:c.1784-435_1784-434del , LRG_85t1:c.1784-435_1784-434del NP_005582.1:n.1784-435_1784-434del
XM_005274008.2:c.1316-435_1316-434del XP_005274065.1:n.1316-435_1316-434del
XM_006718842.2:c.1784-438_1784-437del XP_006718905.1:n.1784-438_1784-437del
XM_011542837.1:c.1784-435_1784-434del XP_011541139.1:n.1784-435_1784-434del
XR_947828.1:n.2080-435_2080-434del
NM_001330347.1:c.1784-438_1784-437del NP_001317276.1:n.1784-438_1784-437del
XM_005274008.3:c.1316-435_1316-434del XP_005274065.1:n.1316-435_1316-434del
XM_006718842.3:c.1784-438_1784-437del XP_006718905.1:n.1784-438_1784-437del
XM_011542837.2:c.1784-435_1784-434del XP_011541139.1:n.1784-435_1784-434del
XM_017017772.1:c.1784-435_1784-434del XP_016873261.1:n.1784-435_1784-434del
XR_947828.2:n.2080-435_2080-434del
NM_001330347.2:c.1784-438_1784-437del NP_001317276.1:n.1784-438_1784-437del
NM_005590.4:c.1783+891_1783+892del NP_005581.2:n.1783+891_1783+892del
NM_005591.4:c.1784-435_1784-434del MANE Select NP_005582.1:n.1784-435_1784-434del