Canonical Allele Identifier: CA226537284
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs878947748

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94478703del , CM000673.2:g.94478703del GRCh38
NC_000011.9:g.94211869del , CM000673.1:g.94211869del GRCh37
NC_000011.8:g.93851517del NCBI36
NG_007261.1:g.20172del , LRG_85:g.20172del

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.544+32del MANE Select ENSP00000325863.4:n.544+32del
ENST00000323929.7:c.544+32del ENSP00000325863.3:n.544+32del
ENST00000323977.7:c.544+32del ENSP00000326094.3:n.544+32del
ENST00000393241.8:c.544+32del ENSP00000376933.4:n.544+32del
ENST00000407439.7:c.553+32del ENSP00000385614.3:n.553+32del
ENST00000540013.5:c.544+32del ENSP00000440986.1:n.544+32del
NM_005590.3:c.544+32del NP_005581.2:n.544+32del
NM_005591.3:c.544+32del , LRG_85t1:c.544+32del NP_005582.1:n.544+32del
XM_005274008.2:c.76+32del XP_005274065.1:n.76+32del
XM_006718842.2:c.544+32del XP_006718905.1:n.544+32del
XM_011542837.1:c.544+32del XP_011541139.1:n.544+32del
XR_947828.1:n.840+32del
NM_001330347.1:c.544+32del NP_001317276.1:n.544+32del
XM_005274008.3:c.76+32del XP_005274065.1:n.76+32del
XM_006718842.3:c.544+32del XP_006718905.1:n.544+32del
XM_011542837.2:c.544+32del XP_011541139.1:n.544+32del
XM_017017772.1:c.544+32del XP_016873261.1:n.544+32del
XR_947828.2:n.840+32del
NM_001330347.2:c.544+32del NP_001317276.1:n.544+32del
NM_005590.4:c.544+32del NP_005581.2:n.544+32del
NM_005591.4:c.544+32del MANE Select NP_005582.1:n.544+32del