Canonical Allele Identifier: CA1992433469
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1946859857

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94476439_94476441del , CM000673.2:g.94476439_94476441del GRCh38
NC_000011.9:g.94209605_94209607del , CM000673.1:g.94209605_94209607del GRCh37
NC_000011.8:g.93849253_93849255del NCBI36
NG_007261.1:g.22436_22438del , LRG_85:g.22436_22438del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.545-36_545-34del MANE Select ENSP00000325863.4:n.545-36_545-34del
ENST00000323929.7:c.545-36_545-34del ENSP00000325863.3:n.545-36_545-34del
ENST00000323977.7:c.545-36_545-34del ENSP00000326094.3:n.545-36_545-34del
ENST00000393241.8:c.545-36_545-34del ENSP00000376933.4:n.545-36_545-34del
ENST00000407439.7:c.554-36_554-34del ENSP00000385614.3:n.554-36_554-34del
ENST00000540013.5:c.545-36_545-34del ENSP00000440986.1:n.545-36_545-34del
NM_005590.3:c.545-36_545-34del NP_005581.2:n.545-36_545-34del
NM_005591.3:c.545-36_545-34del , LRG_85t1:c.545-36_545-34del NP_005582.1:n.545-36_545-34del
XM_005274008.2:c.77-36_77-34del XP_005274065.1:n.77-36_77-34del
XM_006718842.2:c.545-36_545-34del XP_006718905.1:n.545-36_545-34del
XM_011542837.1:c.545-36_545-34del XP_011541139.1:n.545-36_545-34del
XR_947828.1:n.841-36_841-34del
NM_001330347.1:c.545-36_545-34del NP_001317276.1:n.545-36_545-34del
XM_005274008.3:c.77-36_77-34del XP_005274065.1:n.77-36_77-34del
XM_006718842.3:c.545-36_545-34del XP_006718905.1:n.545-36_545-34del
XM_011542837.2:c.545-36_545-34del XP_011541139.1:n.545-36_545-34del
XM_017017772.1:c.545-36_545-34del XP_016873261.1:n.545-36_545-34del
XR_947828.2:n.841-36_841-34del
NM_001330347.2:c.545-36_545-34del NP_001317276.1:n.545-36_545-34del
NM_005590.4:c.545-36_545-34del NP_005581.2:n.545-36_545-34del
NM_005591.4:c.545-36_545-34del MANE Select NP_005582.1:n.545-36_545-34del