Canonical Allele Identifier: CA941023246
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1945929388

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94446315_94446317del , CM000673.2:g.94446315_94446317del GRCh38
NC_000011.9:g.94179481_94179483del , CM000673.1:g.94179481_94179483del GRCh37
NC_000011.8:g.93819129_93819131del NCBI36
NG_007261.1:g.52560_52562del , LRG_85:g.52560_52562del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1784-422_1784-420del MANE Select ENSP00000325863.4:n.1784-422_1784-420del
ENST00000323929.7:c.1784-422_1784-420del ENSP00000325863.3:n.1784-422_1784-420del
ENST00000323977.7:c.1783+904_1783+906del ENSP00000326094.3:n.1783+904_1783+906del
ENST00000393241.8:c.1784-425_1784-423del ENSP00000376933.4:n.1784-425_1784-423del
ENST00000407439.7:c.1793-422_1793-420del ENSP00000385614.3:n.1793-422_1793-420del
ENST00000535120.1:n.83-425_83-423del
NM_005590.3:c.1783+904_1783+906del NP_005581.2:n.1783+904_1783+906del
NM_005591.3:c.1784-422_1784-420del , LRG_85t1:c.1784-422_1784-420del NP_005582.1:n.1784-422_1784-420del
XM_005274008.2:c.1316-422_1316-420del XP_005274065.1:n.1316-422_1316-420del
XM_006718842.2:c.1784-425_1784-423del XP_006718905.1:n.1784-425_1784-423del
XM_011542837.1:c.1784-422_1784-420del XP_011541139.1:n.1784-422_1784-420del
XR_947828.1:n.2080-422_2080-420del
NM_001330347.1:c.1784-425_1784-423del NP_001317276.1:n.1784-425_1784-423del
XM_005274008.3:c.1316-422_1316-420del XP_005274065.1:n.1316-422_1316-420del
XM_006718842.3:c.1784-425_1784-423del XP_006718905.1:n.1784-425_1784-423del
XM_011542837.2:c.1784-422_1784-420del XP_011541139.1:n.1784-422_1784-420del
XM_017017772.1:c.1784-422_1784-420del XP_016873261.1:n.1784-422_1784-420del
XR_947828.2:n.2080-422_2080-420del
NM_001330347.2:c.1784-425_1784-423del NP_001317276.1:n.1784-425_1784-423del
NM_005590.4:c.1783+904_1783+906del NP_005581.2:n.1783+904_1783+906del
NM_005591.4:c.1784-422_1784-420del MANE Select NP_005582.1:n.1784-422_1784-420del