Canonical Allele Identifier: CA2615588083
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94459394_94459398del , CM000673.2:g.94459394_94459398del GRCh38
NC_000011.9:g.94192560_94192564del , CM000673.1:g.94192560_94192564del GRCh37
NC_000011.8:g.93832208_93832212del NCBI36
NG_007261.1:g.39478_39482del , LRG_85:g.39478_39482del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1500+11_1500+15del MANE Select ENSP00000325863.4:n.1500+11_1500+15del
ENST00000323929.7:c.1500+11_1500+15del ENSP00000325863.3:n.1500+11_1500+15del
ENST00000323977.7:c.1500+11_1500+15del ENSP00000326094.3:n.1500+11_1500+15del
ENST00000393241.8:c.1500+11_1500+15del ENSP00000376933.4:n.1500+11_1500+15del
ENST00000407439.7:c.1509+11_1509+15del ENSP00000385614.3:n.1509+11_1509+15del
NM_005590.3:c.1500+11_1500+15del NP_005581.2:n.1500+11_1500+15del
NM_005591.3:c.1500+11_1500+15del , LRG_85t1:c.1500+11_1500+15del NP_005582.1:n.1500+11_1500+15del
XM_005274008.2:c.1032+11_1032+15del XP_005274065.1:n.1032+11_1032+15del
XM_006718842.2:c.1500+11_1500+15del XP_006718905.1:n.1500+11_1500+15del
XM_011542837.1:c.1500+11_1500+15del XP_011541139.1:n.1500+11_1500+15del
XR_947828.1:n.1796+11_1796+15del
NM_001330347.1:c.1500+11_1500+15del NP_001317276.1:n.1500+11_1500+15del
XM_005274008.3:c.1032+11_1032+15del XP_005274065.1:n.1032+11_1032+15del
XM_006718842.3:c.1500+11_1500+15del XP_006718905.1:n.1500+11_1500+15del
XM_011542837.2:c.1500+11_1500+15del XP_011541139.1:n.1500+11_1500+15del
XM_017017772.1:c.1500+11_1500+15del XP_016873261.1:n.1500+11_1500+15del
XR_947828.2:n.1796+11_1796+15del
NM_001330347.2:c.1500+11_1500+15del NP_001317276.1:n.1500+11_1500+15del
NM_005590.4:c.1500+11_1500+15del NP_005581.2:n.1500+11_1500+15del
NM_005591.4:c.1500+11_1500+15del MANE Select NP_005582.1:n.1500+11_1500+15del